A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703467



Internal ID15440119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121434324..121476358hg38UCSC Ensembl
Innerchr10:123193838..123235872hg19UCSC Ensembl
Innerchr10:123183828..123225862hg18UCSC Ensembl
Innerchr10:123183828..123225862hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3842035
hg1942035
hg1842035
hg1742035
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527088
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703467
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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