A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13864474



Internal ID3866290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76099567..76100903hg38UCSC Ensembl
Innerchr10:76099774..76100696hg38UCSC Ensembl
Outerchr10:76099360..76101110hg38UCSC Ensembl
chr10:77859325..77860661hg19UCSC Ensembl
Innerchr10:77859532..77860454hg19UCSC Ensembl
Outerchr10:77859118..77860868hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg381337
hg191337
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623859
Supporting Variants
SamplesNA20359
Known GenesC10orf11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13864474
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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