A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593348



Internal ID16380757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1870705..1871691hg38UCSC Ensembl
Innerchr4:1872432..1873418hg19UCSC Ensembl
Innerchr4:1842230..1843216hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38987
hg19987
hg18987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv988462
Samples
Known GenesWHSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593348
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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