A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17541347



Internal ID21865702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112831383..112834131hg38UCSC Ensembl
chr5:112167080..112169828hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg382749
hg192749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017599
Supporting Variants
Samples
Known GenesAPC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17541347
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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