A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520746



Internal ID15448039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74501830..74982098hg38UCSC Ensembl
Innerchr6:75211546..75691814hg19UCSC Ensembl
Innerchr6:75268266..75748534hg18UCSC Ensembl
Innerchr6:75268266..75748534hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38480269
hg19480269
hg18480269
hg17480269
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697587
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520746
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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