A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3345917



Internal ID15192901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99507505..100072784hg38UCSC Ensembl
Innerchr5:99509495..100071204hg38UCSC Ensembl
Outerchr5:99507395..100072904hg38UCSC Ensembl
chr5:98843209..99408488hg19UCSC Ensembl
Innerchr5:98845199..99406908hg19UCSC Ensembl
Outerchr5:98843099..99408608hg19UCSC Ensembl
chr5:98871108..99436387hg18UCSC Ensembl
Innerchr5:98873098..99434807hg18UCSC Ensembl
Outerchr5:98870998..99436507hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38565280
hg19565280
hg18565280
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv8809346
SamplesNA12878
Known Genes
MethodSequencing
Analysis
Platform454
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)esv3345917
Frequency
Sample Size185
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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