A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2841373



Internal ID15404628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14805077..14811820hg38UCSC Ensembl
Innerchr19:14915889..14922632hg19UCSC Ensembl
Innerchr19:14776889..14783632hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg386744
hg196744
hg186744
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514890
Supporting Variants
SamplesNA19175
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2841373
Frequency
Sample Size2366
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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