A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596284



Internal ID16383693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:179317194..179440207hg38UCSC Ensembl
Innerchr4:180238348..180361361hg19UCSC Ensembl
Innerchr4:180475342..180598355hg18UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg38123014
hg19123014
hg18123014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153262
Samples1780854023_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596284
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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