A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1022210



Internal ID16316166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1839384..1892645hg38UCSC Ensembl
Innerchr5:1839498..1892759hg19UCSC Ensembl
Innerchr5:1892498..1945759hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3853262
hg1953262
hg1853262
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596893
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)nssv1022210
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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