A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626703



Internal ID7013534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67075285..67077493hg38UCSC Ensembl
Innerchr11:67075295..67077483hg38UCSC Ensembl
Outerchr11:67075275..67077503hg38UCSC Ensembl
chr11:66842756..66844964hg19UCSC Ensembl
Innerchr11:66842766..66844954hg19UCSC Ensembl
Outerchr11:66842746..66844974hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg382209
hg192209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14197388, essv14197390, essv14197380, essv14197392, essv14197389, essv14197387, essv14197391, essv14197385, essv14197393, essv14197386, essv14197384, essv14197379, essv14197382, essv14197381, essv14197383
SamplesHG00358, NA20802, NA12751, HG02687, HG00330, HG03986, NA12489, HG00344, HG01941, NA20876, HG02494, NA19732, HG03703, HG00234, NA12006
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626703
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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