A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8671762



Internal ID13707697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26564016..26564071hg38UCSC Ensembl
Innerchr10:26564034..26564053hg38UCSC Ensembl
Outerchr10:26563998..26564089hg38UCSC Ensembl
chr10:26852945..26853000hg19UCSC Ensembl
Innerchr10:26852963..26852982hg19UCSC Ensembl
Outerchr10:26852927..26853018hg19UCSC Ensembl
chr10:26892951..26893006hg18UCSC Ensembl
Innerchr10:26892969..26892988hg18UCSC Ensembl
Outerchr10:26892933..26893024hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3851
hg1951
hg1851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3327751
Supporting Variants
SamplesNA12891
Known GenesAPBB1IP
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8671762
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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