A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578953



Internal ID16019676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:21403995..21426805hg38UCSC Ensembl
Innerchr19:21586797..21609607hg19UCSC Ensembl
Innerchr19:21378637..21401447hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3822811
hg1922811
hg1822811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6320n54
Supporting Variantsnssv896582
Samples
Known GenesZNF493
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578953
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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