A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626707



Internal ID6666855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67139805..67149822hg38UCSC Ensembl
Innerchr11:67139809..67149819hg38UCSC Ensembl
Outerchr11:67139802..67149826hg38UCSC Ensembl
chr11:66907276..66917293hg19UCSC Ensembl
Innerchr11:66907280..66917290hg19UCSC Ensembl
Outerchr11:66907273..66917297hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3810018
hg1910018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14197400, essv14197397, essv14197396, essv14197399, essv14197398, essv14197401
SamplesHG00367, HG00232, HG01684, HG00324, NA11894, HG00269
Known GenesKDM2A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626707
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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