A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17170611



Internal ID21474121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:26158446..26158774hg38UCSC Ensembl
chrY:28304593..28304921hg19UCSC Ensembl
CytobandYq11.23
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5671987
Supporting Variants
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17170611
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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