A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593911



Internal ID16381320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34157314..34286927hg38UCSC Ensembl
Innerchr4:34158936..34288549hg19UCSC Ensembl
Innerchr4:33835331..33964944hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38129614
hg19129614
hg18129614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8997n54
Supporting Variantsnssv995206
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593911
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer