A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700716



Internal ID15090682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13015403..13015482hg38UCSC Ensembl
Innerchr10:13057403..13057482hg19UCSC Ensembl
Innerchr10:13097409..13097488hg18UCSC Ensembl
Innerchr10:13097409..13097488hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3880
hg1980
hg1880
hg1780
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516198
Supporting Variants
Samples
Known GenesCCDC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700716
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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