A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17165891



Internal ID21429897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:146382747..146382747hg38UCSC Ensembl
chrX:145464265..145464265hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5616507
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17165891
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