A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578614



Internal ID16019337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11230959..11265999hg38UCSC Ensembl
Innerchr19:11341635..11376675hg19UCSC Ensembl
Innerchr19:11202635..11237675hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3835041
hg1935041
hg1835041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893550, nssv893549, nssv893548
Samples
Known GenesC19orf80, DOCK6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578614
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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