A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3965n100



Internal ID22790052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:89186243..90282526hg38UCSC Ensembl
chr2:89485727..90321385hg19UCSC Ensembl
chr2:89266842..89958690hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381096284
hg19835659
hg18691849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012225, nsv1012878, nsv1004236, nsv1013894, nsv997591, nsv1006291, nsv1006976, nsv999797, nsv1002782, nsv1005911, nsv1013367, nsv1002507, nsv1002696, nsv1009269, nsv999088, nsv1009695, nsv1007428, nsv1014069, nsv1001439, nsv1009276, nsv1013138, nsv1010319, nsv1011467, nsv1004659, nsv1002259, nsv1000440, nsv1010733, nsv1005841, nsv1003969, nsv1012149, nsv1006329, nsv1012585, nsv1002684, nsv1001193
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)dgv3965n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss72
Observed Complex0
Frequencyn/a


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