A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6441n54



Internal ID22774336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39894797..39895316hg38UCSC Ensembl
chr19:40385437..40385956hg19UCSC Ensembl
chr19:45077277..45077796hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38520
hg19520
hg18520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv579519, nsv579516, nsv579517
Samples
Known GenesFCGBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6441n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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