A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738309



Internal ID161975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6883345..6884182hg38UCSC Ensembl
chrY:6751386..6752223hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5430707
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738309
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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