A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517796



Internal ID15445089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24051611..24073945hg38UCSC Ensembl
Innerchr7:24091230..24113564hg19UCSC Ensembl
Innerchr7:24057755..24080089hg18UCSC Ensembl
Innerchr7:23864470..23886804hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3822335
hg1922335
hg1822335
hg1722335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv414n21
Supporting Variantsnssv694058
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517796
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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