A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593837



Internal ID16381246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:25555935..25576891hg38UCSC Ensembl
Innerchr4:25557557..25578513hg19UCSC Ensembl
Innerchr4:25166655..25187611hg18UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3820957
hg1920957
hg1820957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8985n54
Supporting Variantsnssv1152906, nssv994416
SamplesHGDP00154
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593837
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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