A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258409



Internal ID21397909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:149591230..149670926hg38UCSC Ensembl
chrX:148672886..148752594hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3879697
hg1979709
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730128
Supporting Variants
SamplesHG00512
Known GenesHSFX1, HSFX2, TMEM185A
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258409
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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