A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625956



Internal ID6666104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:36484986..36487132hg38UCSC Ensembl
Innerchr11:36484987..36487132hg38UCSC Ensembl
Outerchr11:36484986..36487133hg38UCSC Ensembl
chr11:36506536..36508682hg19UCSC Ensembl
Innerchr11:36506537..36508682hg19UCSC Ensembl
Outerchr11:36506536..36508683hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382147
hg192147
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14091295, essv14091310, essv14091302, essv14091300, essv14091307, essv14091308, essv14091303, essv14091311, essv14091299, essv14091304, essv14091306, essv14091301, essv14091296, essv14091298, essv14091305, essv14091297, essv14091309
SamplesNA19703, HG02798, NA19920, HG03074, HG03479, NA19904, HG01242, HG02885, HG03195, HG03058, HG03048, HG02511, NA19236, NA18879, HG02884, NA19711, HG02284
Known GenesTRAF6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625956
Frequency
Sample Size2504
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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