A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17742839



Internal ID166505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:19767186..19767383hg38UCSC Ensembl
chrY:21929072..21929269hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17742839
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000934


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