A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1022178



Internal ID16316134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1523225..1523782hg38UCSC Ensembl
Innerchr5:1523340..1523897hg19UCSC Ensembl
Innerchr5:1576340..1576897hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38558
hg19558
hg18558
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596880
Supporting Variants
Samples
Known GenesLPCAT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1022178
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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