A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610349



Internal ID6997266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110133004..110136053hg38UCSC Ensembl
Innerchr6:110133030..110136027hg38UCSC Ensembl
Outerchr6:110132978..110136079hg38UCSC Ensembl
chr6:110454207..110457256hg19UCSC Ensembl
Innerchr6:110454233..110457230hg19UCSC Ensembl
Outerchr6:110454181..110457282hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383050
hg193050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12501305, essv12501304, essv12501306
SamplesNA21099, NA20896, HG03469
Known GenesWASF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610349
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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