A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3377747



Internal ID15224720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:9811464..9973186hg38UCSC Ensembl
Innerchr6:9813454..9971606hg38UCSC Ensembl
Outerchr6:9811354..9973306hg38UCSC Ensembl
chr6:9811697..9973419hg19UCSC Ensembl
Innerchr6:9813687..9971839hg19UCSC Ensembl
Outerchr6:9811587..9973539hg19UCSC Ensembl
chr6:9919683..10081405hg18UCSC Ensembl
Innerchr6:9921673..10079825hg18UCSC Ensembl
Outerchr6:9919573..10081525hg18UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38161723
hg19161723
hg18161723
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8809409
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3377747
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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