A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13351541



Internal ID4892204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139498172..139600722hg38UCSC Ensembl
Innerchr8:139498313..139600581hg38UCSC Ensembl
Outerchr8:139498031..139600863hg38UCSC Ensembl
chr8:140510415..140612965hg19UCSC Ensembl
Innerchr8:140510556..140612824hg19UCSC Ensembl
Outerchr8:140510274..140613106hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38102551
hg19102551
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3619019
Supporting Variants
SamplesNA12414
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13351541
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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