A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524011



Internal ID15451304
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699871
Samples
Known GenesUBR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524011
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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