A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169014



Internal ID21466833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:10083411..10083481hg38UCSC Ensembl
chrY:9921020..9921090hg19UCSC Ensembl
CytobandYp11.2
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667687
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169014
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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