A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17548037



Internal ID21872392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112764170..112764170hg38UCSC Ensembl
chr5:112099867..112099867hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073386
Supporting Variants
Samples
Known GenesAPC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17548037
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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