A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7752700



Internal ID13813865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72420970..72420971hg38UCSC Ensembl
Innerchr11:72420901..72421040hg38UCSC Ensembl
Outerchr11:72420900..72421041hg38UCSC Ensembl
chr11:72132014..72132015hg19UCSC Ensembl
Innerchr11:72131945..72132084hg19UCSC Ensembl
Outerchr11:72131944..72132085hg19UCSC Ensembl
chr11:71809662..71809663hg18UCSC Ensembl
Innerchr11:71809732..71809593hg18UCSC Ensembl
Outerchr11:71809592..71809733hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38151
hg19151
hg18151
Variant TypeCNV mobile element insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3303142
Supporting Variants
SamplesNA18505
Known GenesCLPB
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv7752700
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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