A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2171n100



Internal ID22788258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:19811063..19998696hg38UCSC Ensembl
chr15:20016316..20203949hg19UCSC Ensembl
chr15:18276329..18463963hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38187634
hg19187634
hg18187635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036442, nsv1049114
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)dgv2171n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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