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nsv3114516

  • Variant Calls:21
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,787

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 186 SVs from 49 studies. See in: genome view    
Remapped(Score: Perfect):47,915,569-47,920,355Question Mark
Overlapping variant regions from other studies: 186 SVs from 49 studies. See in: genome view    
Submitted genomic48,207,766-48,212,552Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv3114516RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000015.10Chr1547,915,56947,920,355
nsv3114516Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000015.9Chr1548,207,76648,212,552

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv14095275deletionsample5Oligo aCGHProbe signal intensity69
nssv14095294deletionsample14Oligo aCGHProbe signal intensity61
nssv14095942deletionsample28Oligo aCGHProbe signal intensity68
nssv14095950deletionsample33Oligo aCGHProbe signal intensity71
nssv14096119deletionsample127Oligo aCGHProbe signal intensity60
nssv14096164deletionsample148Oligo aCGHProbe signal intensity80
nssv14096217deletionsample171Oligo aCGHProbe signal intensity83
nssv14097044deletionsample259Oligo aCGHProbe signal intensity86
nssv14097067deletionsample272Oligo aCGHProbe signal intensity54
nssv14097071deletionsample274Oligo aCGHProbe signal intensity73
nssv14097127deletionsample312Oligo aCGHProbe signal intensity89
nssv14097130deletionsample313Oligo aCGHProbe signal intensity80
nssv14097184deletionsample353Oligo aCGHProbe signal intensity46
nssv14097216deletionsample373Oligo aCGHProbe signal intensity100
nssv14097504deletionsample191Oligo aCGHProbe signal intensity68
nssv14097520deletionsample200Oligo aCGHProbe signal intensity73
nssv14097527deletionsample203Oligo aCGHProbe signal intensity88
nssv14098145deletionsample395Oligo aCGHProbe signal intensity85
nssv14098154deletionsample400Oligo aCGHProbe signal intensity92
nssv14098162deletionsample403Oligo aCGHProbe signal intensity69
nssv14098195deletionsample421Oligo aCGHProbe signal intensity52

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv14095275RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14095294RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14095942RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14095950RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14096119RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14096164RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14096217RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14097044RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14097067RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14097071RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14097127RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14097130RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14097184RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14097216RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14097504RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14097520RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14097527RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14098145RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14098154RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14098162RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14098195RemappedPerfectNC_000015.10:g.(?_
47915569)_(4792035
5_?)del
GRCh38.p12First PassNC_000015.10Chr1547,915,56947,920,355
nssv14095275Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14095294Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14095942Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14095950Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14096119Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14096164Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14096217Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14097044Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14097067Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14097071Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14097127Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14097130Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14097184Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14097216Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14097504Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14097520Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14097527Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14098145Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14098154Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14098162Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552
nssv14098195Submitted genomicNC_000015.9:g.(?_4
8207766)_(48212552
_?)del
GRCh37 (hg19)NC_000015.9Chr1548,207,76648,212,552

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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