A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv894556



Internal ID15841826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:13097863..13109362hg38UCSC Ensembl
Innerchr19:13208677..13220176hg19UCSC Ensembl
Innerchr19:13069677..13081176hg18UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg3811500
hg1911500
hg1811500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578635
Supporting Variants
Samples
Known GenesLYL1, NFIX, TRMT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv894556
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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