A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738411



Internal ID162077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12225678..12226640hg38UCSC Ensembl
chrY:14346383..14347345hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38963
hg19963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414058
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738411
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002188


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