A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6418n54



Internal ID18998594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35268614..35270070hg38UCSC Ensembl
chr19:35759517..35760973hg19UCSC Ensembl
chr19:40451357..40452813hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381457
hg191457
hg181457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579398, nsv579395, nsv579399, nsv579397
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6418n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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