A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17151291



Internal ID21423875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142970296..142970296hg38UCSC Ensembl
chr8:144051713..144051713hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635806
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17151291
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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