A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258773



Internal ID21400110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149723540..149788478hg38UCSC Ensembl
chrX:148805200..148870140hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3864939
hg1964941
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesNA19238
Known GenesHSFX1, HSFX2, MAGEA9, MAGEA9B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258773
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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