A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169549



Internal ID21406332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1173940..1174355hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666730
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169549
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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