A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1021163



Internal ID16315119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:467509..473113hg38UCSC Ensembl
Innerchr5:467624..473228hg19UCSC Ensembl
Innerchr5:520624..526228hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg385605
hg195605
hg185605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596639
Supporting Variants
Samples
Known GenesPP7080
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1021163
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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