A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522856



Internal ID15450149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32449402..32469805hg38UCSC Ensembl
Innerchr3:32490894..32511297hg19UCSC Ensembl
Innerchr3:32465898..32486301hg18UCSC Ensembl
Innerchr3:32465898..32486301hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3820404
hg1920404
hg1820404
hg1720404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698510
Samples
Known GenesCMTM7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522856
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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