A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3858n100



Internal ID22789945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:59394636..59440818hg38UCSC Ensembl
chr2:59621771..59667953hg19UCSC Ensembl
chr2:59475275..59521457hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3846183
hg1946183
hg1846183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014000, nsv1005536
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)dgv3858n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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