A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17171294



Internal ID21431787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:569957..569957hg38UCSC Ensembl
chrY:480692..480692hg19UCSC Ensembl
CytobandYp11.32
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5606477
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17171294
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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