A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6069165



Internal ID21978398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20729380..20729380hg38UCSC Ensembl
chr4:20731003..20731003hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537682
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6069165
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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