A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423437



Internal ID202458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10238188..10245238hg38UCSC Ensembl
chrY:10075797..10082847hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg387051
hg197051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738350
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423437
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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