A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596296



Internal ID16383705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:180605774..181150989hg38UCSC Ensembl
Innerchr4:181526927..182072142hg19UCSC Ensembl
Innerchr4:181763921..182309136hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38545216
hg19545216
hg18545216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1017058
Samples
Known GenesLINC00290
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596296
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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