A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3732n100



Internal ID22789819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:17039813..17067611hg38UCSC Ensembl
chr2:17221080..17248878hg19UCSC Ensembl
chr2:17084561..17112359hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3827799
hg1927799
hg1827799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999846, nsv997651, nsv1004296, nsv1008682
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)dgv3732n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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