A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578611



Internal ID16019334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10102342..10103231hg38UCSC Ensembl
Innerchr19:10213018..10213907hg19UCSC Ensembl
Innerchr19:10074018..10074907hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38890
hg19890
hg18890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6266n54
Supporting Variantsnssv893545
Samples
Known GenesANGPTL6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578611
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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