A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169486



Internal ID21410459
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1887944..1887944hg38UCSC Ensembl
chrY:1956837..1956837hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623042
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169486
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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