A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677672



Internal ID15414324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64041842..64051525hg38UCSC Ensembl
Innerchr16:64075746..64085429hg19UCSC Ensembl
Innerchr16:62633247..62642930hg18UCSC Ensembl
Innerchr16:62633247..62642930hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg389684
hg199684
hg189684
hg179684
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516354
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677672
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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