A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974332



Internal ID22749267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10172802..10184386hg38UCSC Ensembl
chrY:10010411..10021995hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3811585
hg1911585
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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