A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596092



Internal ID16383501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167395597..167557494hg38UCSC Ensembl
Innerchr4:168316748..168478645hg19UCSC Ensembl
Innerchr4:168553323..168715220hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38161898
hg19161898
hg18161898
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152842
Samples1780862576_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596092
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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