A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697790



Internal ID15434442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:11383484..11405316hg38UCSC Ensembl
Innerchr16:11477341..11499172hg19UCSC Ensembl
Innerchr16:11384842..11406673hg18UCSC Ensembl
Innerchr16:11384842..11406673hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3821833
hg1921832
hg1821832
hg1721832
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521106
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697790
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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