A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170493



Internal ID21507841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26578028..26578334hg38UCSC Ensembl
chrY:28724175..28724481hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5666238
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170493
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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