A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17737429



Internal ID161095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:122016930..122016930hg38UCSC Ensembl
chrX:121150783..121150783hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg381179
hg191179
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5541840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17737429
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0123301


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer