A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257849



Internal ID21399838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:63159232..63249804hg38UCSC Ensembl
chrX:62378699..62469681hg19UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg3890573
hg1990983
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730051
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257849
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