A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619740



Internal ID7006614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13734351..13755888hg38UCSC Ensembl
Innerchr9:13734493..13755746hg38UCSC Ensembl
Outerchr9:13734209..13756030hg38UCSC Ensembl
chr9:13734350..13755887hg19UCSC Ensembl
Innerchr9:13734492..13755745hg19UCSC Ensembl
Outerchr9:13734208..13756029hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3821538
hg1921538
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13407045, essv13407041, essv13407043, essv13407042, essv13407038, essv13407044, essv13407040, essv13407039
SamplesHG00881, HG02382, HG00717, HG01599, HG01847, NA18630, HG00698, HG00595
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619740
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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