A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152890



Internal ID15855573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25552889..25576891hg38UCSC Ensembl
Innerchr4:25554511..25578513hg19UCSC Ensembl
Innerchr4:25163609..25187611hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3824003
hg1924003
hg1824003
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593829
Supporting Variants
Samples1782681110_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152890
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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