A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068418



Internal ID21977651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122799110..122799110hg38UCSC Ensembl
chr5:122134805..122134805hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg382584
hg192584
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17538608
Samples
Known GenesSNX2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068418
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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