A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1021237



Internal ID16315193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:472511..473651hg38UCSC Ensembl
Innerchr5:472626..473766hg19UCSC Ensembl
Innerchr5:525626..526766hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381141
hg191141
hg181141
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596679
Supporting Variants
Samples
Known GenesPP7080, SLC9A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1021237
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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