A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17743006



Internal ID166672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56673388..56771388hg38UCSC Ensembl
chrY:58819483..58917483hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg3898001
hg1998001
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423441
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17743006
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.5


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