A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695144



Internal ID15085110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:33266591..33367332hg38UCSC Ensembl
Innerchr1:33732192..33832933hg19UCSC Ensembl
Innerchr1:33504779..33605520hg18UCSC Ensembl
Innerchr1:33401285..33502026hg17UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38100742
hg19100742
hg18100742
hg17100742
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522364
Supporting Variants
Samples
Known GenesA3GALT2, MIR3605, PHC2, ZNF362
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695144
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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