A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705588



Internal ID15442240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:13977396..14004283hg38UCSC Ensembl
Innerchr16:14071253..14098140hg19UCSC Ensembl
Innerchr16:13978754..14005641hg18UCSC Ensembl
Innerchr16:13978754..14005641hg17UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3826888
hg1926888
hg1826888
hg1726888
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528904
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705588
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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