A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2588n100



Internal ID20154204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44801821..45008646hg38UCSC Ensembl
chr15:45094019..45300844hg19UCSC Ensembl
chr15:42881311..43088136hg18UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38206826
hg19206826
hg18206826
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048867, nsv1048668, nsv1040140, nsv1053041, nsv1036204, nsv1047353, nsv1041613, nsv1040940
Samples
Known GenesC15orf43
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2588n100
Frequency
Sample Size29084
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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