A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521077



Internal ID15448370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:69504952..69569453hg38UCSC Ensembl
Innerchr6:70214844..70279345hg19UCSC Ensembl
Innerchr6:70271565..70336066hg18UCSC Ensembl
Innerchr6:70271565..70336066hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3864502
hg1964502
hg1864502
hg1764502
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697772
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521077
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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