A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034745



Internal ID90886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50874187..50874327hg38UCSC Ensembl
chr10:52633947..52634087hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478401
Supporting Variants
Samples
Known GenesA1CF
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034745
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002654


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