A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738407



Internal ID162073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:12085661..12087066hg38UCSC Ensembl
chrY:14206367..14207772hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415619
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738407
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001563


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