A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv456e214



Internal ID22756350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:81666909..81795106hg38UCSC Ensembl
chr15:81959250..82087447hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38128198
hg19128198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3637041, esv3637039
SamplesNA19089
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv456e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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