A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579353



Internal ID16020076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34481093..34482768hg38UCSC Ensembl
Innerchr19:34971998..34973673hg19UCSC Ensembl
Innerchr19:39663838..39665513hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381676
hg191676
hg181676
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6408n54
Supporting Variantsnssv898587, nssv898586
Samples
Known GenesWTIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579353
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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