A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578316



Internal ID16019039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1622785..1629081hg38UCSC Ensembl
Innerchr19:1622784..1629080hg19UCSC Ensembl
Innerchr19:1573784..1580080hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386297
hg196297
hg186297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6205n54
Supporting Variantsnssv891843
Samples
Known GenesTCF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578316
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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