A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891839



Internal ID15839109
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 StatusS
Merged Variantsnsv578313
Supporting Variants
Samples
Known GenesTCF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891839
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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