A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738422



Internal ID162088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12930280..12936590hg38UCSC Ensembl
chrY:15042190..15048499hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg386311
hg196310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414331
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738422
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00188088


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