A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1040482



Internal ID15893668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:114781684..114807732hg38UCSC Ensembl
Innerchr5:114117381..114143429hg19UCSC Ensembl
Innerchr5:114145280..114171328hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3826049
hg1926049
hg1826049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv599447
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)nssv1040482
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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