A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626903



Internal ID6667051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78525196..78659627hg38UCSC Ensembl
Innerchr11:78525346..78659477hg38UCSC Ensembl
Outerchr11:78525046..78659777hg38UCSC Ensembl
chr11:78236242..78370672hg19UCSC Ensembl
Innerchr11:78236392..78370522hg19UCSC Ensembl
Outerchr11:78236092..78370822hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38134432
hg19134431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv211e214
Supporting Variantsessv14215360, essv14215357, essv14215358, essv14215354, essv14215356, essv14215353, essv14215362, essv14215359, essv14215363, essv14215355, essv14215361
SamplesHG00142, HG02784, HG03895, HG03837, HG03644, HG03672, HG03019, NA20888, NA20852, HG02778, HG03989
Known GenesNARS2, TENM4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626903
Frequency
Sample Size2504
Observed Gain11
Observed Loss0
Observed Complex0
Frequencyn/a


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