A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626650



Internal ID6666800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63687487..63692635hg38UCSC Ensembl
Innerchr11:63687487..63692635hg38UCSC Ensembl
Outerchr11:63687372..63692762hg38UCSC Ensembl
chr11:63454959..63460107hg19UCSC Ensembl
Innerchr11:63454959..63460107hg19UCSC Ensembl
Outerchr11:63454844..63460234hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385149
hg195149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14184862, essv14184863
SamplesNA19020, NA19380
Known GenesRTN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626650
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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