A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596624



Internal ID16037347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:391653..392348hg38UCSC Ensembl
Innerchr5:391768..392463hg19UCSC Ensembl
Innerchr5:444768..445463hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38696
hg19696
hg18696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9478n54
Supporting Variantsnssv1021069
Samples
Known GenesAHRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596624
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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