A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597814



Internal ID16038537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:35855308..35858900hg38UCSC Ensembl
Innerchr5:35855410..35859002hg19UCSC Ensembl
Innerchr5:35891167..35894759hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg383593
hg193593
hg183593
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1028951
Samples
Known GenesIL7R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597814
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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