A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891842



Internal ID15839112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1622459..1628972hg38UCSC Ensembl
Innerchr19:1622458..1628971hg19UCSC Ensembl
Innerchr19:1573458..1579971hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg386514
hg196514
hg186514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578315
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)nssv891842
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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