A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527079



Internal ID15454372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33959534..33976237hg38UCSC Ensembl
Innerchr6:33927311..33944014hg19UCSC Ensembl
Innerchr6:34035289..34051992hg18UCSC Ensembl
Innerchr6:34035289..34051992hg17UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3816704
hg1916704
hg1816704
hg1716704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703458
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527079
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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