A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891239



Internal ID15838509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:811362..812545hg38UCSC Ensembl
Innerchr19:811362..812545hg19UCSC Ensembl
Innerchr19:762362..763545hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381184
hg191184
hg181184
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578171
Supporting Variants
Samples
Known GenesLPPR3, PTBP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891239
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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