A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3926n100



Internal ID22790013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88831228..89245848hg38UCSC Ensembl
chr2:89130741..89545331hg19UCSC Ensembl
chr2:88911856..89326446hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38414621
hg19414591
hg18414591
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009277, nsv997748, nsv1009052, nsv1010239, nsv998817, nsv1000641, nsv1008416, nsv1005696, nsv998097, nsv1012313, nsv1007435, nsv1013480, nsv1000244, nsv999890, nsv997604, nsv1007002, nsv997410, nsv1002296, nsv1006126, nsv1010079, nsv999040, nsv1005971, nsv1001098, nsv1009858, nsv1007743
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3926n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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