A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600326



Internal ID16387735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:174523067..174609230hg38UCSC Ensembl
Innerchr5:173950070..174036233hg19UCSC Ensembl
Innerchr5:173882676..173968839hg18UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3886164
hg1986164
hg1886164
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1045665
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600326
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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