A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv658147



Internal ID15394799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4296025..4345104hg38UCSC Ensembl
Innerchr17:4199320..4248399hg19UCSC Ensembl
Innerchr17:4146069..4195148hg18UCSC Ensembl
Innerchr17:4146069..4195148hg17UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3849080
hg1949080
hg1849080
hg1749080
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515940
Supporting Variants
Samples
Known GenesUBE2G1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv658147
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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