A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170680



Internal ID21473618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:323839..323839hg38UCSC Ensembl
chrY:234574..234574hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3829634
hg1929634
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5614850
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170680
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