A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579313



Internal ID16020036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32716739..32720911hg38UCSC Ensembl
Innerchr19:33207645..33211817hg19UCSC Ensembl
Innerchr19:37899485..37903657hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384173
hg194173
hg184173
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898323, nssv898322, nssv898324, nssv898325
Samples
Known GenesTDRD12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579313
Frequency
Sample Size17421
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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