A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256162



Internal ID21399960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149578221..149672560hg38UCSC Ensembl
chrX:148659877..148754228hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3894340
hg1994352
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, TMEM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256162
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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