A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738323



Internal ID161989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7835808..7844097hg38UCSC Ensembl
chrY:7703849..7712138hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg388290
hg198290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426389
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738323
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000626566


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