A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626505



Internal ID6666655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57642468..57654301hg38UCSC Ensembl
Innerchr11:57642618..57654151hg38UCSC Ensembl
Outerchr11:57642318..57654451hg38UCSC Ensembl
chr11:57409941..57421773hg19UCSC Ensembl
Innerchr11:57410091..57421623hg19UCSC Ensembl
Outerchr11:57409791..57421923hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811834
hg1911833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14168719
SamplesHG03491
Known GenesYPEL4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626505
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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