A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672489



Internal ID21620794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12418752..12419252hg38UCSC Ensembl
chrY:14530551..14531051hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17169596
SamplesHG03009
Known GenesGYG2P1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672489
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