A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593910



Internal ID16381319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34141502..34270180hg38UCSC Ensembl
Innerchr4:34143124..34271802hg19UCSC Ensembl
Innerchr4:33819519..33948197hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38128679
hg19128679
hg18128679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8997n54
Supporting Variantsnssv995204, nssv995205
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593910
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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