A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730223



Internal ID21401034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55181489..55183046hg38UCSC Ensembl
chrX:55207922..55209479hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg381558
hg191558
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16257277
SamplesNA19240
Known GenesMTRNR2L10
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nsv4730223
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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