A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683209



Internal ID15073175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80924545..80968018hg38UCSC Ensembl
Innerchr16:80958442..81001915hg19UCSC Ensembl
Innerchr16:79515943..79559416hg18UCSC Ensembl
Innerchr16:79515943..79559416hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3843474
hg1943474
hg1843474
hg1743474
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520122
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683209
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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