A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3976n100



Internal ID22790063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:89896137..90228225hg38UCSC Ensembl
chr2:89934947..90267091hg19UCSC Ensembl
chr2:89571989..89904396hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38332089
hg19332145
hg18332408
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012751, nsv1006485, nsv997519, nsv1002979
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)dgv3976n100
Frequency
Sample Size11257
Observed Gain14
Observed Loss270
Observed Complex0
Frequencyn/a


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