A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702477



Internal ID15439129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:74839615..74956163hg38UCSC Ensembl
Innerchr16:74873513..74990061hg19UCSC Ensembl
Innerchr16:73431014..73547562hg18UCSC Ensembl
Innerchr16:73431014..73547562hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38116549
hg19116549
hg18116549
hg17116549
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526213
Supporting Variants
Samples
Known GenesWDR59
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702477
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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