A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578606



Internal ID16019329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10061840..10102478hg38UCSC Ensembl
Innerchr19:10172516..10213154hg19UCSC Ensembl
Innerchr19:10033516..10074154hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3840639
hg1940639
hg1840639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150642
SamplesNINDS_165
Known GenesANGPTL6, C19orf66, C3P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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