A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623859



Internal ID6664026
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13864469, essv13864464, essv13864473, essv13864462, essv13864472, essv13864470, essv13864468, essv13864460, essv13864475, essv13864474, essv13864461, essv13864465, essv13864467, essv13864458, essv13864471, essv13864459, essv13864466, essv13864463
SamplesNA18520, NA19222, HG02983, HG03304, NA19223, NA20342, NA20362, NA19144, HG03538, HG03079, HG02595, NA19153, HG02337, HG03352, HG03446, HG03343, HG02678, NA20359
Known GenesC10orf11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623859
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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