A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17152860



Internal ID21460094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28501976..28501976hg38UCSC Ensembl
chr6:28469753..28469753hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641293
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17152860
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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