A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521185



Internal ID15101792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:16195077..16239548hg38UCSC Ensembl
Innerchr6:16195308..16239779hg19UCSC Ensembl
Innerchr6:16303287..16347758hg18UCSC Ensembl
Innerchr6:16303287..16347758hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3844472
hg1944472
hg1844472
hg1744472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697833
Samples
Known GenesGMPR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521185
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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