A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1023682



Internal ID16317638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:3594565..3597716hg38UCSC Ensembl
Innerchr5:3594679..3597830hg19UCSC Ensembl
Innerchr5:3647679..3650830hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg383152
hg193152
hg183152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596925
Supporting Variants
Samples
Known GenesIRX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1023682
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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