A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899262



Internal ID15846532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39642185..39819857hg38UCSC Ensembl
Innerchr19:40132825..40310497hg19UCSC Ensembl
Innerchr19:44824665..45002337hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38177673
hg19177673
hg18177673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579511
Supporting Variants
Samples
Known GenesCLC, LEUTX, LGALS14, LGALS16, LGALS17A, LOC100129935
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899262
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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