A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738318



Internal ID161984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:7529460..7533678hg38UCSC Ensembl
chrY:7397501..7401719hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg384219
hg194219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433165
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738318
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00375


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