A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv171e214



Internal ID22756065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124267163..124270758hg38UCSC Ensembl
chr10:125955732..125959327hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383596
hg193596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3624805, esv3624804
SamplesHG01441, HG00306, HG01369, HG01378
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv171e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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