A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5980126



Internal ID22755061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12252309..12264730hg38UCSC Ensembl
chrY:14373013..14385434hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg3812422
hg1912422
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5980126
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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