A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17146978



Internal ID21486461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:159845843..159845843hg38UCSC Ensembl
chr6:160266875..160266875hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635262
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17146978
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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