A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6542n54



Internal ID20139966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54052839..54056151hg38UCSC Ensembl
chr19:54556093..54559405hg19UCSC Ensembl
chr19:59247905..59251217hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383313
hg193313
hg183313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580119, nsv580129, nsv580123, nsv580116, nsv580118, nsv580124, nsv580117
Samples
Known GenesVSTM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6542n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer