A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596037



Internal ID16383446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:164481157..164938799hg38UCSC Ensembl
Innerchr4:165402309..165859951hg19UCSC Ensembl
Innerchr4:165621759..166079401hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38457643
hg19457643
hg18457643
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1010739
Samples
Known GenesLOC100505989, LOC100506013, MIR5684
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596037
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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