A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675086



Internal ID15411738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75194071..75272504hg38UCSC Ensembl
Innerchr16:75227969..75306402hg19UCSC Ensembl
Innerchr16:73785470..73863903hg18UCSC Ensembl
Innerchr16:73785470..73863903hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3878434
hg1978434
hg1878434
hg1778434
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516504
Supporting Variants
Samples
Known GenesBCAR1, CTRB1, CTRB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675086
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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