A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073386



Internal ID21982619
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 StatusM
Merged Variants
Supporting Variantsnssv17548037
Samples
Known GenesAPC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073386
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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