A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108338



Internal ID22017571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:29316572..29576308hg38UCSC Ensembl
chr5:29316679..29576415hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38259737
hg19259737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555805
Samples
Known GenesLOC101929681
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108338
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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