A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597811



Internal ID16385220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:35270458..35305567hg38UCSC Ensembl
Innerchr5:35270560..35305669hg19UCSC Ensembl
Innerchr5:35306317..35341426hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3835110
hg1935110
hg1835110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1028948
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597811
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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