A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738341



Internal ID162007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:9836388..9841388hg38UCSC Ensembl
chrY:9673997..9678997hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg385001
hg195001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5424895
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738341
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001261


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