A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523812



Internal ID15451105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:127318574..127321479hg38UCSC Ensembl
Innerchr7:126958628..126961533hg19UCSC Ensembl
Innerchr7:126745864..126748769hg18UCSC Ensembl
Innerchr7:126552579..126555484hg17UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg382906
hg192906
hg182906
hg172906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699642
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523812
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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