A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169552



Internal ID21410434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1174677..1174884hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5669002
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169552
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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