A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526717



Internal ID21851075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:46776357..46776357hg38UCSC Ensembl
chr1:47242029..47242029hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054184
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526717
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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