A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525696



Internal ID15106303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170130646..170187139hg38UCSC Ensembl
Innerchr6:170445870..170502363hg19UCSC Ensembl
Innerchr6:170287795..170344288hg18UCSC Ensembl
Innerchr6:170363502..170419995hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3856494
hg1956494
hg1856494
hg1756494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701856
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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