A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519690



Internal ID15446983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131994531..132029904hg38UCSC Ensembl
Innerchr7:131679290..131714663hg19UCSC Ensembl
Innerchr7:131329830..131365203hg18UCSC Ensembl
Innerchr7:131136545..131171918hg17UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3835374
hg1935374
hg1835374
hg1735374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696994
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519690
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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