A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6408n54



Internal ID22774303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:34480941..34482768hg38UCSC Ensembl
chr19:34971846..34973673hg19UCSC Ensembl
chr19:39663686..39665513hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg381828
hg191828
hg181828
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579348, nsv579351, nsv579353, nsv579352, nsv579350
Samples
Known GenesWTIP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6408n54
Frequency
Sample Size17421
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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