A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5996729



Internal ID21906072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21446612..21486946hg38UCSC Ensembl
chr4:21448235..21488569hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3840335
hg1940335
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541572
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5996729
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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