A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597262



Internal ID16384671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:14943347..15044733hg38UCSC Ensembl
Innerchr5:14943456..15044842hg19UCSC Ensembl
Innerchr5:14996456..15097842hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38101387
hg19101387
hg18101387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153527
SamplesHGDP00598
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597262
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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