A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680110



Internal ID15416762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85270375..85270519hg38UCSC Ensembl
Innerchr16:85303981..85304125hg19UCSC Ensembl
Innerchr16:83861482..83861626hg18UCSC Ensembl
Innerchr16:83861482..83861626hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38145
hg19145
hg18145
hg17145
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517320
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680110
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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