A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595905



Internal ID6983223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38157317..38290490hg38UCSC Ensembl
Innerchr3:38157485..38290322hg38UCSC Ensembl
Outerchr3:38157149..38290658hg38UCSC Ensembl
chr3:38198808..38331981hg19UCSC Ensembl
Innerchr3:38198976..38331813hg19UCSC Ensembl
Outerchr3:38198640..38332149hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38133174
hg19133174
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10983706, essv10983707, essv10983705, essv10983704
SamplesHG02375, HG02140, HG02067, HG02166
Known GenesOXSR1, SLC22A13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595905
Frequency
Sample Size2504
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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