A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121409



Internal ID21467385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:169459731..169459731hg38UCSC Ensembl
chr5:168886735..168886735hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5644456
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121409
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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