A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578313



Internal ID16019036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1620999..1629081hg38UCSC Ensembl
Innerchr19:1620998..1629080hg19UCSC Ensembl
Innerchr19:1571998..1580080hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388083
hg198083
hg188083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6205n54
Supporting Variantsnssv891840, nssv891839
Samples
Known GenesTCF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578313
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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