A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256848



Internal ID21400130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149591230..149663655hg38UCSC Ensembl
chrX:148672886..148745324hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3872426
hg1972439
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesNA19238
Known GenesHSFX1, HSFX2, TMEM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256848
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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