A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600195



Internal ID16387604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:164125252..164175746hg38UCSC Ensembl
Innerchr5:163552258..163602752hg19UCSC Ensembl
Innerchr5:163484836..163535330hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3850495
hg1950495
hg1850495
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1045000
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600195
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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