A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108193



Internal ID22017426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17608470..17613741hg38UCSC Ensembl
chrX:17626590..17631861hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg385272
hg195272
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649302
Samples
Known GenesNHS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108193
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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