A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1021337



Internal ID16315293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:670630..691486hg38UCSC Ensembl
Innerchr5:670745..691601hg19UCSC Ensembl
Innerchr5:723745..744601hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3820857
hg1920857
hg1820857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596715
Supporting Variants
Samples
Known GenesTPPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1021337
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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