A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3357598



Internal ID15204577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84952741..84963492hg38UCSC Ensembl
Innerchr8:84954731..84962077hg38UCSC Ensembl
Outerchr8:84952631..84963612hg38UCSC Ensembl
chr8:85864976..85875727hg19UCSC Ensembl
Innerchr8:85866966..85874247hg19UCSC Ensembl
Outerchr8:85864866..85875847hg19UCSC Ensembl
chr8:86027531..86038562hg18UCSC Ensembl
Innerchr8:86029521..86036982hg18UCSC Ensembl
Outerchr8:86027421..86038682hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3810752
hg1910752
hg1811032
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8809538
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3357598
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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