A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578272



Internal ID16018995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1233682..1244776hg38UCSC Ensembl
Innerchr19:1233681..1244775hg19UCSC Ensembl
Innerchr19:1184681..1195775hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811095
hg1911095
hg1811095
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv891775
Samples
Known GenesATP5D, C19orf26
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578272
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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