A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1021213



Internal ID16315169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:467561..474770hg38UCSC Ensembl
Innerchr5:467676..474885hg19UCSC Ensembl
Innerchr5:520676..527885hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg387210
hg197210
hg187210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596655
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)nssv1021213
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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