A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv155n21



Internal ID20131876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79919071..79923673hg38UCSC Ensembl
chr15:80211413..80216015hg19UCSC Ensembl
chr15:77998468..78003070hg18UCSC Ensembl
chr15:77998468..78003070hg17UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg384603
hg194603
hg184603
hg174603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv525035, nsv524197
Samples
Known GenesC15orf37, ST20, ST20-MTHFS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv155n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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