A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13961249



Internal ID3963065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123722001..123735148hg38UCSC Ensembl
Innerchr10:123722206..123734943hg38UCSC Ensembl
Outerchr10:123721796..123735353hg38UCSC Ensembl
chr10:125481517..125494664hg19UCSC Ensembl
Innerchr10:125481722..125494459hg19UCSC Ensembl
Outerchr10:125481312..125494869hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3813148
hg1913148
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624800
Supporting Variants
SamplesNA19068
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13961249
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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