A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17066313



Internal ID21467530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75962621..75962621hg38UCSC Ensembl
chr1:76428306..76428306hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38660
hg19660
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5611855
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17066313
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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