A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17136542



Internal ID21506951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172493389..172493389hg38UCSC Ensembl
chr5:171920393..171920393hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5630062
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17136542
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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