A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520784



Internal ID15101391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:53125208..53126560hg38UCSC Ensembl
Innerchr6:52990006..52991358hg19UCSC Ensembl
Innerchr6:53097965..53099317hg18UCSC Ensembl
Innerchr6:53097965..53099317hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg381353
hg191353
hg181353
hg171353
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697607
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520784
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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