A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17743005



Internal ID166671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26660038..26665888hg38UCSC Ensembl
chrY:28806185..28812035hg19UCSC Ensembl
CytobandYq12
Allele length
AssemblyAllele length
hg385851
hg195851
Variant TypeOTHER copy number variation
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5414693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17743005
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.499687


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