A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742580



Internal ID20518564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21291299..21291420hg38UCSC Ensembl
chr4:21292922..21293043hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294459
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742580
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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