A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616238



Internal ID21808285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18875033..18930111hg38UCSC Ensembl
chr13:19449173..19504251hg19UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg3855079
hg1955079
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106790
Supporting Variants
Samples
Known GenesLINC00408
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616238
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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