A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596625



Internal ID16037348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:391653..392411hg38UCSC Ensembl
Innerchr5:391768..392526hg19UCSC Ensembl
Innerchr5:444768..445526hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38759
hg19759
hg18759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9478n54
Supporting Variantsnssv1021070
Samples
Known GenesAHRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596625
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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