A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17166123



Internal ID21463349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154140895..154140895hg38UCSC Ensembl
chrX:153406369..153406369hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg384383
hg194383
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5609085
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17166123
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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