A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3860n100



Internal ID20155476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63318463..63379554hg38UCSC Ensembl
chr2:63545598..63606689hg19UCSC Ensembl
chr2:63399102..63460193hg18UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3861092
hg1961092
hg1861092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014935, nsv1013613, nsv1012628
Samples
Known GenesWDPCP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3860n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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