A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523747



Internal ID15451040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45529506..45558870hg38UCSC Ensembl
Innerchr7:45569105..45598469hg19UCSC Ensembl
Innerchr7:45535630..45564994hg18UCSC Ensembl
Innerchr7:45342345..45371709hg17UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3829365
hg1929365
hg1829365
hg1729365
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699564
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523747
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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