A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528433



Internal ID15455726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:82906803..82943983hg38UCSC Ensembl
Innerchr6:83616522..83653702hg19UCSC Ensembl
Innerchr6:83673241..83710421hg18UCSC Ensembl
Innerchr6:83673241..83710421hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3837181
hg1937181
hg1837181
hg1737181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705026
Samples
Known GenesUBE3D
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528433
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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