A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258343



Internal ID21399389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:6218792..6220368hg38UCSC Ensembl
chrX:6136833..6138409hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg381577
hg191577
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730244
Supporting Variants
SamplesHG00732
Known GenesNLGN4X
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258343
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