A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174262



Internal ID15879491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89921587..90538186hg38UCSC Ensembl
Innerchr10:91681344..92297943hg19UCSC Ensembl
Innerchr10:91671324..92287923hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38616600
hg19616600
hg18616600
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551875
Supporting Variants
SamplesHGDP01374
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174262
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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