A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256901



Internal ID21400056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153070523..153079542hg38UCSC Ensembl
chrX:152238906..152247925hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg389020
hg199020
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730132
Supporting Variants
SamplesNA19238
Known GenesPNMA6A, PNMA6C
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256901
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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