A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174990



Internal ID15872921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65012286..65372541hg38UCSC Ensembl
Innerchr10:66772044..67132299hg19UCSC Ensembl
Innerchr10:66442050..66802305hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38360256
hg19360256
hg18360256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551232
Supporting Variants
SamplesHGDP00076
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174990
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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