A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256900



Internal ID21398026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154581225..154633196hg38UCSC Ensembl
chrX:153809488..153861459hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3851972
hg1951972
Variant TypeOTHER inversion
Copy Number
Allele StateHemizygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730207
Supporting Variants
SamplesHG00512
Known GenesCTAG1A, CTAG1B, FAM223A, FAM223B
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256900
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