A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704707



Internal ID15441359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:65984569..65994585hg38UCSC Ensembl
Innerchr16:66018472..66028488hg19UCSC Ensembl
Innerchr16:64575973..64585989hg18UCSC Ensembl
Innerchr16:64575973..64585989hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3810017
hg1910017
hg1810017
hg1710017
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528159
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704707
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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