A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3862n100



Internal ID20155478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68727253..68771874hg38UCSC Ensembl
chr2:68954385..68999006hg19UCSC Ensembl
chr2:68807889..68852510hg18UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg3844622
hg1944622
hg1844622
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006929, nsv1009266
Samples
Known GenesARHGAP25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3862n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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