A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6104996



Internal ID22014230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:135725991..135935861hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38209871
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637701
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6104996
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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