A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2595n100



Internal ID20154211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51964903..52049904hg38UCSC Ensembl
chr15:52257100..52342101hg19UCSC Ensembl
chr15:50044392..50129393hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3885002
hg1985002
hg1885002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047260, nsv1050664
Samples
Known GenesLEO1, MAPK6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2595n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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