A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258705



Internal ID21399434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:51692394..51727337hg38UCSC Ensembl
chrX:51435432..51470433hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3834944
hg1935002
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730130
Supporting Variants
SamplesHG00732
Known GenesCENPVP1, CENPVP2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258705
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