A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415661



Internal ID194914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:17607988..17646123hg38UCSC Ensembl
chrY:19719868..19758003hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3838136
hg1938136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415661
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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