A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519889



Internal ID15100496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156751681..156788667hg38UCSC Ensembl
Innerchr6:157072815..157109801hg19UCSC Ensembl
Innerchr6:157114507..157151493hg18UCSC Ensembl
Innerchr6:157164928..157201914hg17UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3836987
hg1936987
hg1836987
hg1736987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697108
Samples
Known GenesARID1B, MIR4466
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519889
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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