A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13909025



Internal ID3910841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:98019700..98021991hg38UCSC Ensembl
Innerchr10:98019882..98021809hg38UCSC Ensembl
Outerchr10:98019518..98022173hg38UCSC Ensembl
chr10:99779457..99781748hg19UCSC Ensembl
Innerchr10:99779639..99781566hg19UCSC Ensembl
Outerchr10:99779275..99781930hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg382292
hg192292
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624329
Supporting Variants
SamplesNA18636
Known GenesCRTAC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13909025
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