A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705366



Internal ID15442018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75888272..75963452hg38UCSC Ensembl
Innerchr16:75922170..75997350hg19UCSC Ensembl
Innerchr16:74479671..74554851hg18UCSC Ensembl
Innerchr16:74479671..74554851hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3875181
hg1975181
hg1875181
hg1775181
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528716
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705366
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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