A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738400



Internal ID162066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11727388..11735388hg38UCSC Ensembl
chrY:13848094..13856094hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138809
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738400
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.999255


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