A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8778n54



Internal ID22776673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188759802..188815021hg38UCSC Ensembl
chr3:188477590..188532809hg19UCSC Ensembl
chr3:189960284..190015503hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3855220
hg1955220
hg1855220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv592762, nsv592761
Samples
Known GenesLPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8778n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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