A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5421022



Internal ID200111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18869638..18878788hg38UCSC Ensembl
chrY:21031524..21040674hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg389151
hg199151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742827
Samples
Known GenesNCRNA00185
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5421022
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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