A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593900



Internal ID16381309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:31721374..31807078hg38UCSC Ensembl
Innerchr4:31722996..31808700hg19UCSC Ensembl
Innerchr4:31332094..31417795hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3885705
hg1985705
hg1885702
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv995198
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593900
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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