A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522696



Internal ID15449989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24167409..24183905hg38UCSC Ensembl
Innerchr7:24207028..24223524hg19UCSC Ensembl
Innerchr7:24173553..24190049hg18UCSC Ensembl
Innerchr7:23980268..23996764hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3816497
hg1916497
hg1816497
hg1716497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706106
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522696
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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