A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3691n100



Internal ID22789778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12772..86644hg38UCSC Ensembl
chr2:12772..86644hg19UCSC Ensembl
chr2:2772..76644hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3873873
hg1973873
hg1873873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999544, nsv1005795, nsv1012054, nsv999983, nsv1000679, nsv1009879
Samples
Known GenesFAM110C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3691n100
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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