A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13866400



Internal ID4132473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:76712914..76814151hg38UCSC Ensembl
Innerchr10:76713055..76814010hg38UCSC Ensembl
Outerchr10:76712773..76814292hg38UCSC Ensembl
chr10:78472672..78573909hg19UCSC Ensembl
Innerchr10:78472813..78573768hg19UCSC Ensembl
Outerchr10:78472531..78574050hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38101238
hg19101238
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623871
Supporting Variants
SamplesHG03744
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13866400
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer