A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578610



Internal ID16019333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10102342..10103112hg38UCSC Ensembl
Innerchr19:10213018..10213788hg19UCSC Ensembl
Innerchr19:10074018..10074788hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38771
hg19771
hg18771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893544
Samples
Known GenesANGPTL6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578610
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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