U.S. flag

An official website of the United States government

nsv3169611

  • Variant Calls:13
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:14,355

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 723 SVs from 80 studies. See in: genome view    
Remapped(Score: Perfect):3,919,342-3,933,696Question Mark
Overlapping variant regions from other studies: 723 SVs from 80 studies. See in: genome view    
Remapped(Score: Perfect):3,776,864-3,791,218Question Mark
Overlapping variant regions from other studies: 341 SVs from 27 studies. See in: genome view    
Submitted genomic3,764,272-3,778,626Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv3169611RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000008.11Chr83,919,3423,926,6653,932,5843,933,696
nsv3169611RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000008.10Chr83,776,8643,784,1873,790,1063,791,218
nsv3169611Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000008.9Chr83,764,2723,771,5953,777,5143,778,626

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisCopy numberOther Calls in this Sample and Study
nssv14246616duplicationNGO_32SNP arraySNP genotyping analysis4153
nssv14249303deletionMLY_11SNP arraySNP genotyping analysis1128
nssv14249615deletionNGO_9SNP arraySNP genotyping analysis1137
nssv14243791deletionNGO_24SNP arraySNP genotyping analysis0155
nssv14244897deletionNGO_23SNP arraySNP genotyping analysis0127
nssv14246286deletionSNI_3SNP arraySNP genotyping analysis0121
nssv14246875deletionSNI_15SNP arraySNP genotyping analysis0132
nssv14247072deletionSNI_14SNP arraySNP genotyping analysis0136
nssv14247805deletionNGO_10SNP arraySNP genotyping analysis0137
nssv14247975deletionNGO_19SNP arraySNP genotyping analysis0107
nssv14248290deletionNGO_42SNP arraySNP genotyping analysis0116
nssv14249836deletionNGO_36SNP arraySNP genotyping analysis0128
nssv14252109deletionSNI_11SNP arraySNP genotyping analysis0129

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv14246616RemappedPerfectNC_000008.11:g.(39
19342_3926665)_(39
32584_3933696)dup
GRCh38.p12First PassNC_000008.11Chr83,919,3423,926,6653,932,5843,933,696
nssv14249303RemappedPerfectNC_000008.11:g.(39
19342_3926665)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,919,3423,926,6653,932,5843,933,696
nssv14249615RemappedPerfectNC_000008.11:g.(39
19342_3926665)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,919,3423,926,6653,932,5843,933,696
nssv14243791RemappedPerfectNC_000008.11:g.(39
26665_3929538)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,926,6653,929,5383,932,5843,933,696
nssv14244897RemappedPerfectNC_000008.11:g.(39
26665_3929538)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,926,6653,929,5383,932,5843,933,696
nssv14246286RemappedPerfectNC_000008.11:g.(39
26665_3929538)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,926,6653,929,5383,932,5843,933,696
nssv14246875RemappedPerfectNC_000008.11:g.(39
26665_3929538)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,926,6653,929,5383,932,5843,933,696
nssv14247072RemappedPerfectNC_000008.11:g.(39
26665_3929538)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,926,6653,929,5383,932,5843,933,696
nssv14247805RemappedPerfectNC_000008.11:g.(39
26665_3929538)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,926,6653,929,5383,932,5843,933,696
nssv14247975RemappedPerfectNC_000008.11:g.(39
26665_3929538)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,926,6653,929,5383,932,5843,933,696
nssv14248290RemappedPerfectNC_000008.11:g.(39
26665_3929538)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,926,6653,929,5383,932,5843,933,696
nssv14249836RemappedPerfectNC_000008.11:g.(39
26665_3929538)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,926,6653,929,5383,932,5843,933,696
nssv14252109RemappedPerfectNC_000008.11:g.(39
26665_3929538)_(39
32584_3933696)del
GRCh38.p12First PassNC_000008.11Chr83,926,6653,929,5383,932,5843,933,696
nssv14246616RemappedPerfectNC_000008.10:g.(37
76864_3784187)_(37
90106_3791218)dup
GRCh37.p13First PassNC_000008.10Chr83,776,8643,784,1873,790,1063,791,218
nssv14249303RemappedPerfectNC_000008.10:g.(37
76864_3784187)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,776,8643,784,1873,790,1063,791,218
nssv14249615RemappedPerfectNC_000008.10:g.(37
76864_3784187)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,776,8643,784,1873,790,1063,791,218
nssv14243791RemappedPerfectNC_000008.10:g.(37
84187_3787060)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,784,1873,787,0603,790,1063,791,218
nssv14244897RemappedPerfectNC_000008.10:g.(37
84187_3787060)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,784,1873,787,0603,790,1063,791,218
nssv14246286RemappedPerfectNC_000008.10:g.(37
84187_3787060)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,784,1873,787,0603,790,1063,791,218
nssv14246875RemappedPerfectNC_000008.10:g.(37
84187_3787060)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,784,1873,787,0603,790,1063,791,218
nssv14247072RemappedPerfectNC_000008.10:g.(37
84187_3787060)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,784,1873,787,0603,790,1063,791,218
nssv14247805RemappedPerfectNC_000008.10:g.(37
84187_3787060)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,784,1873,787,0603,790,1063,791,218
nssv14247975RemappedPerfectNC_000008.10:g.(37
84187_3787060)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,784,1873,787,0603,790,1063,791,218
nssv14248290RemappedPerfectNC_000008.10:g.(37
84187_3787060)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,784,1873,787,0603,790,1063,791,218
nssv14249836RemappedPerfectNC_000008.10:g.(37
84187_3787060)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,784,1873,787,0603,790,1063,791,218
nssv14252109RemappedPerfectNC_000008.10:g.(37
84187_3787060)_(37
90106_3791218)del
GRCh37.p13First PassNC_000008.10Chr83,784,1873,787,0603,790,1063,791,218
nssv14246616Submitted genomicNC_000008.9:g.(376
4272_3771595)_(377
7514_3778626)dup
NCBI36 (hg18)NC_000008.9Chr83,764,2723,771,5953,777,5143,778,626
nssv14249303Submitted genomicNC_000008.9:g.(376
4272_3771595)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,764,2723,771,5953,777,5143,778,626
nssv14249615Submitted genomicNC_000008.9:g.(376
4272_3771595)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,764,2723,771,5953,777,5143,778,626
nssv14243791Submitted genomicNC_000008.9:g.(377
1595_3774468)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,771,5953,774,4683,777,5143,778,626
nssv14244897Submitted genomicNC_000008.9:g.(377
1595_3774468)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,771,5953,774,4683,777,5143,778,626
nssv14246286Submitted genomicNC_000008.9:g.(377
1595_3774468)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,771,5953,774,4683,777,5143,778,626
nssv14246875Submitted genomicNC_000008.9:g.(377
1595_3774468)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,771,5953,774,4683,777,5143,778,626
nssv14247072Submitted genomicNC_000008.9:g.(377
1595_3774468)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,771,5953,774,4683,777,5143,778,626
nssv14247805Submitted genomicNC_000008.9:g.(377
1595_3774468)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,771,5953,774,4683,777,5143,778,626
nssv14247975Submitted genomicNC_000008.9:g.(377
1595_3774468)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,771,5953,774,4683,777,5143,778,626
nssv14248290Submitted genomicNC_000008.9:g.(377
1595_3774468)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,771,5953,774,4683,777,5143,778,626
nssv14249836Submitted genomicNC_000008.9:g.(377
1595_3774468)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,771,5953,774,4683,777,5143,778,626
nssv14252109Submitted genomicNC_000008.9:g.(377
1595_3774468)_(377
7514_3778626)del
NCBI36 (hg18)NC_000008.9Chr83,771,5953,774,4683,777,5143,778,626

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

Support Center