A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524331



Internal ID15451624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18515745..18522089hg38UCSC Ensembl
Innerchr6:18515976..18522320hg19UCSC Ensembl
Innerchr6:18623955..18630299hg18UCSC Ensembl
Innerchr6:18623955..18630299hg17UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg386345
hg196345
hg186345
hg176345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700237
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524331
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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