A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv144n21



Internal ID20131865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26513916..26649934hg38UCSC Ensembl
chr15:26759063..26895081hg19UCSC Ensembl
chr15:24310156..24446174hg18UCSC Ensembl
chr15:24310156..24446174hg17UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38136019
hg19136019
hg18136019
hg17136019
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv525893, nsv524934
Samples
Known GenesGABRB3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv144n21
Frequency
Sample Size2026
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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