A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1021167



Internal ID15968437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:467509..473253hg38UCSC Ensembl
Innerchr5:467624..473368hg19UCSC Ensembl
Innerchr5:520624..526368hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg385745
hg195745
hg185745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596640
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)nssv1021167
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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