A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742951



Internal ID166617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:21006688..21014188hg38UCSC Ensembl
chrY:23168574..23176074hg19UCSC Ensembl
CytobandYq11.223
Allele length
AssemblyAllele length
hg387501
hg197501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431383
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742951
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00125865


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