A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699871



Internal ID15436523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42538361..42693666hg38UCSC Ensembl
Innerchr6:42506099..42661404hg19UCSC Ensembl
Innerchr6:42614077..42769382hg18UCSC Ensembl
Innerchr6:42614077..42769382hg17UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38155306
hg19155306
hg18155306
hg17155306
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524011
Supporting Variants
Samples
Known GenesUBR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699871
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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