A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1022117



Internal ID16316073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1178659..1180310hg38UCSC Ensembl
Innerchr5:1178774..1180425hg19UCSC Ensembl
Innerchr5:1231774..1233425hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg381652
hg191652
hg181652
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596846
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1022117
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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