A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653562



Internal ID15043528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16041829..16054087hg38UCSC Ensembl
Innerchr1:16368324..16380582hg19UCSC Ensembl
Innerchr1:16240911..16253169hg18UCSC Ensembl
Innerchr1:16113630..16125888hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3812259
hg1912259
hg1812259
hg1712259
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517651
Supporting Variants
Samples
Known GenesCLCNKB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653562
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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