A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597113



Internal ID16384522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10269823..10274393hg38UCSC Ensembl
Innerchr5:10269935..10274505hg19UCSC Ensembl
Innerchr5:10322935..10327505hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg384571
hg194571
hg184571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1024228
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597113
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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