A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432095



Internal ID210851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10227238..10246738hg38UCSC Ensembl
chrY:10064847..10084347hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3819501
hg1919501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738348
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432095
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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