A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1022208



Internal ID16316164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1822212..1880777hg38UCSC Ensembl
Innerchr5:1822326..1880891hg19UCSC Ensembl
Innerchr5:1875326..1933891hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3858566
hg1958566
hg1858566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596891
Supporting Variants
Samples
Known GenesIRX4, LOC101929034
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1022208
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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