A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034492



Internal ID90693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45806132..45826948hg38UCSC Ensembl
chr10:46301580..46322396hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3820817
hg1920817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488862
Supporting Variants
Samples
Known GenesAGAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034492
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.011246


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