A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5971036



Internal ID22745971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:20579053..20580702hg38UCSC Ensembl
chrY:22740939..22742588hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg381650
hg191650
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517312
Samples
Known GenesEIF1AY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5971036
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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