A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17167149



Internal ID21457381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:25446172..25446172hg38UCSC Ensembl
chrX:25464289..25464289hg19UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg381833
hg191833
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611807
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17167149
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