A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624329



Internal ID6664496
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13909025
SamplesNA18636
Known GenesCRTAC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624329
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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