A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2316n209



Internal ID22828391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:4756803..4794627hg38UCSC Ensembl
chrY:4624844..4662668hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3837825
hg1937825
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5970919, nsv5979394
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv2316n209
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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