A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169860



Internal ID21508107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:18039453..18040876hg38UCSC Ensembl
chrY:20201339..20202762hg19UCSC Ensembl
CytobandYq11.222
Allele length
AssemblyAllele length
hg381424
hg191424
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666650
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169860
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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