A curated catalogue of human genomic structural variation




Variant Details

Variant: essv8808536



Internal ID13642902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91440195..91445238hg38UCSC Ensembl
Innerchr10:91442185..91443658hg38UCSC Ensembl
Outerchr10:91440085..91445358hg38UCSC Ensembl
chr10:93199952..93204995hg19UCSC Ensembl
Innerchr10:93201942..93203415hg19UCSC Ensembl
Outerchr10:93199842..93205115hg19UCSC Ensembl
chr10:93189932..93194975hg18UCSC Ensembl
Innerchr10:93191922..93193395hg18UCSC Ensembl
Outerchr10:93189822..93195095hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg385044
hg195044
hg185044
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3345260
Supporting Variants
SamplesNA12878
Known GenesHECTD2, LOC100188947
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)essv8808536
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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