A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700865



Internal ID15437517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:11440050..11442946hg38UCSC Ensembl
Innerchr10:11482049..11484945hg19UCSC Ensembl
Innerchr10:11522055..11524951hg18UCSC Ensembl
Innerchr10:11522055..11524951hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382897
hg192897
hg182897
hg172897
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515865
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700865
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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