A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033558



Internal ID90064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45695265..45907265hg38UCSC Ensembl
chr10:46190713..46402713hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38212001
hg19212001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485998
Supporting Variants
Samples
Known GenesAGAP4, FAM21C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033558
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003292


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