A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8953496



Internal ID14859317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72420976..72421014hg38UCSC Ensembl
Innerchr11:72420966..72421022hg38UCSC Ensembl
Outerchr11:72420928..72421060hg38UCSC Ensembl
chr11:72132020..72132058hg19UCSC Ensembl
Innerchr11:72132010..72132066hg19UCSC Ensembl
Outerchr11:72131972..72132104hg19UCSC Ensembl
chr11:71809668..71809706hg18UCSC Ensembl
Innerchr11:71809714..71809658hg18UCSC Ensembl
Outerchr11:71809620..71809752hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38178
hg19178
hg18178
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3370613
Supporting Variants
SamplesNA19114
Known GenesCLPB
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8953496
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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