A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257321



Internal ID21399598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72972887..73073289hg38UCSC Ensembl
chrX:72192722..72293128hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg38100403
hg19100407
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730106
Supporting Variants
SamplesHG00733
Known GenesPABPC1L2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257321
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer