A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738314



Internal ID161980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7289153..7289629hg38UCSC Ensembl
chrY:7157194..7157670hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38477
hg19477
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422484
Supporting Variants
Samples
Known GenesPRKY
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738314
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003125


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