A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738307



Internal ID161973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:6786388..6959388hg38UCSC Ensembl
chrY:6654429..6827429hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg38173001
hg19173001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415570
Supporting Variants
Samples
Known GenesAMELY, TBL1Y
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738307
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00251731


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