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nsv3418769

  • Variant Calls:13
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 348 SVs from 42 studies. See in: genome view    
Submitted genomic143,988,243-143,988,243Question Mark
Overlapping variant regions from other studies: 280 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):145,062,411-145,062,411Question Mark
Overlapping variant regions from other studies: 101 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):326,888-326,888Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv3418769Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000008.11Chr8143,988,243143,988,243
nsv3418769RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000008.10Chr8145,062,411145,062,411
nsv3418769RemappedPerfectGRCh37.p13PATCHESFirst PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv14772876alu insertionSAMN04229548Sequencingde novo and local sequence assembly23,009
nssv14772922alu insertionSAMN05603745Sequencingde novo and local sequence assembly27,447
nssv14774016alu insertionSAMN05603729Sequencingde novo and local sequence assembly24,108
nssv14774828alu insertionSAMN03255769Sequencingde novo and local sequence assembly21,134
nssv14775570alu insertionSAMN09651199Sequencingde novo and local sequence assembly27,381
nssv14778153alu insertionSAMN05603847Sequencingde novo and local sequence assembly26,021
nssv14779278alu insertionSAMN09643900Sequencingde novo and local sequence assembly26,631
nssv14779453alu insertionSAMN04229552Sequencingde novo and local sequence assembly24,632
nssv14780597alu insertionSAMN09690649Sequencingde novo and local sequence assembly21,495
nssv14781221alu insertionSAMN06885952Sequencingde novo and local sequence assembly28,070
nssv14784089alu insertionSAMN03838746Sequencingde novo and local sequence assembly26,336
nssv14784186alu insertionSAMN04251426Sequencingde novo and local sequence assembly22,074
nssv14791855alu insertionSAMN02744161Sequencingde novo and local sequence assembly20,941

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv14772876Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14772922Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14774016Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14774828Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14775570Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14778153Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14779278Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14779453Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14780597Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14781221Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14784089Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14784186Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14791855Submitted genomicNC_000008.11:g.143
988243_143988244in
s732
GRCh38 (hg38)NC_000008.11Chr8143,988,243143,988,243
nssv14772876RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14772922RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14774016RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14774828RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14775570RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14778153RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14779278RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14779453RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14780597RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14781221RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14784089RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14784186RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14791855RemappedPerfectNW_003315923.1:g.3
26888_326889ins732
NW_003315923.1:g.3
26888_326889ins732
GRCh37.p13First PassNW_003315923.1Chr8|NW_00
3315923.1
326,888326,888
nssv14772876RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14772922RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14774016RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14774828RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14775570RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14778153RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14779278RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14779453RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14780597RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14781221RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14784089RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14784186RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
nssv14791855RemappedPerfectNC_000008.10:g.145
062411_145062412in
s732NC_000008.10:g
.145062411_1450624
12ins732
GRCh37.p13Second PassNC_000008.10Chr8145,062,411145,062,411
Showing 39 of 65

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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