A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519965



Internal ID15447258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12476544..12524502hg38UCSC Ensembl
Innerchr7:12516170..12564128hg19UCSC Ensembl
Innerchr7:12482695..12530653hg18UCSC Ensembl
Innerchr7:12289410..12337368hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3847959
hg1947959
hg1847959
hg1747959
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv675455, nssv675490, nssv696207, nssv659725, nssv685738
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519965
Frequency
Sample Size2026
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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