A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579311



Internal ID16020034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32708877..32720911hg38UCSC Ensembl
Innerchr19:33199783..33211817hg19UCSC Ensembl
Innerchr19:37891623..37903657hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3812035
hg1912035
hg1812035
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898318
Samples
Known GenesNUDT19, TDRD12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579311
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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