A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4162n100



Internal ID22790249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:209340326..209370838hg38UCSC Ensembl
chr2:210205050..210235562hg19UCSC Ensembl
chr2:209913295..209943807hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3830513
hg1930513
hg1830513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006636, nsv1014900
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)dgv4162n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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