A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112442



Internal ID22021675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:11709537..11710980hg38UCSC Ensembl
chrX:11727657..11729100hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg381444
hg191444
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112442
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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