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nsv3921121

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: Yes
  • Region Size:22,416,207
  • Description:GRCh38/hg38 11q13.5-22.1(chr11:75941754-98357960)x1 AND See cases

Genome View

Select assembly:
Overlapping variant regions from other studies: 56972 SVs from 134 studies. See in: genome view    
Submitted genomic75,941,754-98,357,960Question Mark
Overlapping variant regions from other studies: 56906 SVs from 134 studies. See in: genome view    
Submitted genomic75,652,798-98,228,688Question Mark
Overlapping variant regions from other studies: 15023 SVs from 39 studies. See in: genome view    
Submitted genomic75,330,446-97,733,898Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeAssemblyAssembly UnitSequence IDChrInner StartInner Stop
nsv3921121Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1175,941,75498,357,960
nsv3921121Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000011.9Chr1175,652,79898,228,688
nsv3921121Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000011.8Chr1175,330,44697,733,898

Variant Call Information

Variant Call IDTypeMethodAnalysisSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15161308copy number lossMultipleMultipleSee casesPathogenicClinVarRCV000133838.7, VCV000144356.21

Variant Call Placement Information

Variant Call IDPlacement TypeHGVSAssemblySequence IDChrInner StartInner Stop
nssv15161308Submitted genomicNC_000011.10:g.(?_
75941754)_(9835796
0_?)del
GRCh38 (hg38)NC_000011.10Chr1175,941,75498,357,960
nssv15161308Submitted genomicNC_000011.9:g.(?_7
5652798)_(98228688
_?)del
GRCh37 (hg19)NC_000011.9Chr1175,652,79898,228,688
nssv15161308Submitted genomicNC_000011.8:g.(?_7
5330446)_(97733898
_?)del
NCBI36 (hg18)NC_000011.8Chr1175,330,44697,733,898

No validation data were submitted for this variant

Clinical Assertions

Variant Call IDHGVSTypeAllele OriginSubject PhenotypeClinical InterpretationSource of InterpretationClinVar IDCopy number
nssv15161308GRCh37: NC_000011.9:g.(?_75652798)_(98228688_?)del, GRCh38: NC_000011.10:g.(?_75941754)_(98357960_?)del, NCBI36: NC_000011.8:g.(?_75330446)_(97733898_?)delcopy number lossnot providedSee casesPathogenicClinVarRCV000133838.7, VCV000144356.21

No genotype data were submitted for this variant

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