A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv111e214



Internal ID22756005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36909639..37046972hg38UCSC Ensembl
chr10:37198567..37335900hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38137334
hg19137334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3622940, esv3622939
SamplesHG03445
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv111e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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