A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8687909



Internal ID15038523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125885693..125922491hg38UCSC Ensembl
Innerchr10:125886693..125921491hg38UCSC Ensembl
Outerchr10:125884693..125923491hg38UCSC Ensembl
chr10:127574262..127611060hg19UCSC Ensembl
Innerchr10:127575262..127610060hg19UCSC Ensembl
Outerchr10:127573262..127612060hg19UCSC Ensembl
chr10:127564252..127601050hg18UCSC Ensembl
Innerchr10:127565252..127600050hg18UCSC Ensembl
Outerchr10:127563252..127602050hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg3836799
hg1936799
hg1836799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv3434868
Supporting Variants
SamplesNA19239
Known GenesFANK1
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8687909
Frequency
Sample Size185
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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