A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970919



Internal ID22745854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:4756803..4794459hg38UCSC Ensembl
chrY:4624844..4662500hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3837657
hg1937657
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2316n209
Supporting Variantsnssv17517389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970919
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