A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17065216



Internal ID21443326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37982033..37982033hg38UCSC Ensembl
chr1:38447705..38447705hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5623380
Supporting Variants
SamplesHG00732
Known GenesSF3A3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17065216
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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