A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142324



Internal ID21487113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:146566142..146566142hg38UCSC Ensembl
chr6:146887278..146887278hg19UCSC Ensembl
Cytoband6q24.3
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634557
Supporting Variants
SamplesNA12878
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142324
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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