A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3442671



Internal ID14942938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60874503..60876901hg38UCSC Ensembl
Innerchr11:60875503..60875901hg38UCSC Ensembl
Outerchr11:60873503..60877901hg38UCSC Ensembl
chr11:60641976..60644374hg19UCSC Ensembl
Innerchr11:60642976..60643374hg19UCSC Ensembl
Outerchr11:60640976..60645374hg19UCSC Ensembl
chr11:60398552..60400950hg18UCSC Ensembl
Innerchr11:60399552..60399950hg18UCSC Ensembl
Outerchr11:60397552..60401950hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg382399
hg192399
hg182399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8688460
SamplesNA19239
Known GenesZP1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3442671
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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