A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1022196



Internal ID16316152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:1523276..1523844hg38UCSC Ensembl
Innerchr5:1523391..1523959hg19UCSC Ensembl
Innerchr5:1576391..1576959hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38569
hg19569
hg18569
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv596883
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)nssv1022196
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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