A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256626



Internal ID21399055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:115726295..115729652hg38UCSC Ensembl
chrX:114965484..114971833hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg383358
hg196350
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730056
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256626
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