A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738420



Internal ID162086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12639735..12640236hg38UCSC Ensembl
chrY:14751666..14752167hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5432357
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738420
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00125


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