A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17119507



Internal ID21414570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42715733..42715733hg38UCSC Ensembl
chr21:44135843..44135843hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5670497
Supporting Variants
SamplesHG00513
Known GenesPDE9A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17119507
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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