A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8672156



Internal ID15106996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72420973..72421030hg38UCSC Ensembl
Innerchr11:72420989..72421014hg38UCSC Ensembl
Outerchr11:72420932..72421071hg38UCSC Ensembl
chr11:72132017..72132074hg19UCSC Ensembl
Innerchr11:72132033..72132058hg19UCSC Ensembl
Outerchr11:72131976..72132115hg19UCSC Ensembl
chr11:71809665..71809722hg18UCSC Ensembl
Innerchr11:71809706..71809681hg18UCSC Ensembl
Outerchr11:71809624..71809763hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38174
hg19174
hg18174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3342071
Supporting Variants
SamplesNA19240
Known GenesCLPB
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8672156
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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