A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580089



Internal ID16020812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53419262..53510924hg38UCSC Ensembl
Innerchr19:53922515..54014178hg19UCSC Ensembl
Innerchr19:58614327..58705990hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3891663
hg1991664
hg1891664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n54
Supporting Variantsnssv901168, nssv901170, nssv901169
Samples
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580089
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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