A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17169556



Internal ID21405242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrY:1176329..1176329hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3851
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5624145
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17169556
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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