A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv169e214



Internal ID22756063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121673690..121703457hg38UCSC Ensembl
chr10:123433204..123462971hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3829768
hg1929768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3624756, esv3624757
SamplesHG00306, HG00115, NA19448, NA12156, NA06984, HG01122, NA19982, NA19429
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv169e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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