A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595204



Internal ID16382613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:114408176..114517952hg38UCSC Ensembl
Innerchr4:115329332..115439108hg19UCSC Ensembl
Innerchr4:115548781..115658557hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38109777
hg19109777
hg18109777
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9228n54
Supporting Variantsnssv1152824
SamplesHGDP00579
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595204
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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