A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527794



Internal ID15455087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:20043371..20087938hg38UCSC Ensembl
Innerchr7:20082994..20127561hg19UCSC Ensembl
Innerchr7:20049519..20094086hg18UCSC Ensembl
Innerchr7:19856234..19900801hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3844568
hg1944568
hg1844568
hg1744568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704286
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527794
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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