A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1040351



Internal ID15893537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:112603917..112608752hg38UCSC Ensembl
Innerchr5:111939614..111944449hg19UCSC Ensembl
Innerchr5:111967513..111972348hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg384836
hg194836
hg184836
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599380
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1040351
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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