A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4763808



Internal ID20539668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:20729421..20729421hg38UCSC Ensembl
chr4:20731044..20731044hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16279446
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4763808
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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