A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv371e214



Internal ID22756265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110080127..110111130hg38UCSC Ensembl
chr13:110732474..110763477hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3831004
hg1931004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3633539, esv3633541
SamplesHG01051, HG00641, HG01067, HG01673, HG01187, HG01190, HG01086, HG01105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv371e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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