A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6101096



Internal ID22010329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:79769962..80395600hg38UCSC Ensembl
chr13:80344097..80969735hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38625639
hg19625639
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609604
Samples
Known GenesLINC01080, SPRY2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6101096
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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