A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169551



Internal ID21467431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1174241..1174447hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670725
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169551
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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