A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138331



Internal ID337515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:19063388..19082388hg38UCSC Ensembl
chrY:21225274..21244274hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg3819001
hg1919001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742830
Samples
Known GenesTTTY14
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138331
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