A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030296



Internal ID87908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13742056..13742896hg38UCSC Ensembl
chr10:13784056..13784896hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38841
hg19841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478905
Supporting Variants
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030296
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001717


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