A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125276



Internal ID21410679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:157955966..157955966hg38UCSC Ensembl
chr5:157382974..157382974hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5642171
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125276
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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