A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597614



Internal ID16385023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:25658773..25717398hg38UCSC Ensembl
Innerchr5:25658882..25717507hg19UCSC Ensembl
Innerchr5:25694639..25753264hg18UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg3858626
hg1958626
hg1858626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1027976
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597614
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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