A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2635n100



Internal ID22788722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81703904..81809042hg38UCSC Ensembl
chr15:81996245..82101383hg19UCSC Ensembl
chr15:79783300..79888438hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38105139
hg19105139
hg18105139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046921, nsv1053553, nsv1049781, nsv1045994, nsv1050623, nsv1045058, nsv1049729
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)dgv2635n100
Frequency
Sample Size11257
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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