A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742793



Internal ID166459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:14269506..14304598hg38UCSC Ensembl
chrY:16381386..16416478hg19UCSC Ensembl
CytobandYq11.221
Allele length
AssemblyAllele length
hg3835093
hg1935093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5417684
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742793
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000626566


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