A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138390



Internal ID337574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:17415988..17456388hg38UCSC Ensembl
chrY:19527868..19568268hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3840401
hg1940401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742822
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138390
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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