A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034488



Internal ID90689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45765765..45806265hg38UCSC Ensembl
chr10:46261213..46301713hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3840501
hg1940501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487261
Supporting Variants
Samples
Known GenesFAM21C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034488
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008596


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