A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv597111



Internal ID16384520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:10109273..10139031hg38UCSC Ensembl
Innerchr5:10109385..10139143hg19UCSC Ensembl
Innerchr5:10162385..10192143hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3829759
hg1929759
hg1829759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1024227
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv597111
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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