A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3626698



Internal ID7013529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66809016..66810715hg38UCSC Ensembl
Innerchr11:66809027..66810705hg38UCSC Ensembl
Outerchr11:66809006..66810726hg38UCSC Ensembl
chr11:66576487..66578186hg19UCSC Ensembl
Innerchr11:66576498..66578176hg19UCSC Ensembl
Outerchr11:66576477..66578197hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14195785, essv14195787, essv14195782, essv14195783, essv14195786, essv14195784
SamplesHG03717, HG03718, HG04017, HG02724, HG04152, HG04093
Known GenesC11orf80
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3626698
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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