A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8740712



Internal ID15082788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10906631..10906631hg38UCSC Ensembl
Innerchr11:10906630..10906632hg38UCSC Ensembl
Outerchr11:10906581..10906681hg38UCSC Ensembl
chr11:10928178..10928178hg19UCSC Ensembl
Innerchr11:10928177..10928179hg19UCSC Ensembl
Outerchr11:10928128..10928228hg19UCSC Ensembl
chr11:10884754..10884754hg18UCSC Ensembl
Innerchr11:10884755..10884753hg18UCSC Ensembl
Outerchr11:10884704..10884804hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg381849
hg191849
hg181849
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3441964
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8740712
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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