A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738391



Internal ID162057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:11384779..11384812hg38UCSC Ensembl
chrY:13540455..13540488hg19UCSC Ensembl
CytobandYq11.21
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5558691
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738391
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.723231


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