A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664720



Internal ID15401372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:16542423..16563483hg38UCSC Ensembl
Innerchr10:16584422..16605482hg19UCSC Ensembl
Innerchr10:16624428..16645488hg18UCSC Ensembl
Innerchr10:16624428..16645488hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3821061
hg1921061
hg1821061
hg1721061
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515767
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664720
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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