A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6663n54



Internal ID22774558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3597839..3629432hg38UCSC Ensembl
chr2:3645429..3677022hg19UCSC Ensembl
chr2:3623304..3654897hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3831594
hg1931594
hg1831594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580824, nsv580823
Samples1780862444_A
Known GenesCOLEC11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6663n54
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