A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5666716



Internal ID21615023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:56697030..56697159hg38UCSC Ensembl
chrY:58893712..58893841hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17170998
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5666716
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