A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579312



Internal ID16020035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32716739..32720801hg38UCSC Ensembl
Innerchr19:33207645..33211707hg19UCSC Ensembl
Innerchr19:37899485..37903547hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg384063
hg194063
hg184063
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv898319, nssv898320, nssv898321
Samples
Known GenesTDRD12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579312
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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