A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169943



Internal ID21478626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1674234..1677287hg38UCSC Ensembl
chrY:1743127..1746180hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg383054
hg193054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5665002
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169943
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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