A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066467



Internal ID21409511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:82384713..82384713hg38UCSC Ensembl
chr1:82850396..82850396hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5607843
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066467
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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