A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17145259



Internal ID21421238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66376332..66376332hg38UCSC Ensembl
chr8:67288567..67288567hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633383
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17145259
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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