A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3973n100



Internal ID22790060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:89896137..90091343hg38UCSC Ensembl
chr2:89934947..90130185hg19UCSC Ensembl
chr2:89571989..89767490hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38195207
hg19195239
hg18195502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012741, nsv1007716, nsv1007158, nsv1003890, nsv1006742, nsv1007834, nsv997653, nsv1009176, nsv1004396, nsv1000317, nsv1006245, nsv1002966, nsv1014497
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)dgv3973n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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