A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670150



Internal ID21618457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1314261..1314353hg38UCSC Ensembl
chrY:1383154..1383246hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169260
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670150
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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