A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152204



Internal ID21424265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45643100..45643100hg38UCSC Ensembl
chr6:45610837..45610837hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5631341
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152204
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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