A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415570



Internal ID194826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6786388..6959388hg38UCSC Ensembl
chrY:6654429..6827429hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38173001
hg19173001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738307
Samples
Known GenesAMELY, TBL1Y
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415570
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