A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8670487



Internal ID15056532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:110703286..110703662hg38UCSC Ensembl
Innerchr11:110703442..110703503hg38UCSC Ensembl
Outerchr11:110703127..110703818hg38UCSC Ensembl
chr11:110574009..110574385hg19UCSC Ensembl
Innerchr11:110574165..110574226hg19UCSC Ensembl
Outerchr11:110573850..110574541hg19UCSC Ensembl
chr11:110079219..110079595hg18UCSC Ensembl
Innerchr11:110079375..110079436hg18UCSC Ensembl
Outerchr11:110079060..110079751hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38377
hg19377
hg18377
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3331551
Supporting Variants
SamplesNA19239
Known GenesARHGAP20
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8670487
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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