A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069164



Internal ID21978397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175513147..175513147hg38UCSC Ensembl
chr5:174940150..174940150hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564912
Samples
Known GenesSFXN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069164
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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