A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877403



Internal ID22652368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13119671..13131195hg38UCSC Ensembl
chrY:15231585..15243109hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3811525
hg1911525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455213
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877403
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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