A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2629n100



Internal ID22788716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76586021..76617690hg38UCSC Ensembl
chr15:76878362..76910031hg19UCSC Ensembl
chr15:74665417..74697086hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3831670
hg1931670
hg1831670
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040711, nsv1040450, nsv1048948, nsv1053005
Samples
Known GenesSCAPER
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2629n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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