A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078467



Internal ID21987700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170390516..170390516hg38UCSC Ensembl
chr5:169817520..169817520hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575528
Samples
Known GenesKCNIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078467
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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