A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420499



Internal ID199601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:13114123..13120388hg38UCSC Ensembl
chrY:15226037..15232302hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg386266
hg196266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738424
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420499
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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