A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524123



Internal ID15451416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:199379095..199388384hg38UCSC Ensembl
Innerchr1:199348223..199357512hg19UCSC Ensembl
Innerchr1:197614846..197624135hg18UCSC Ensembl
Innerchr1:196079880..196089169hg17UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg389290
hg199290
hg189290
hg179290
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700001
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524123
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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