A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212859



Internal ID20779899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:21412807..21506981hg38UCSC Ensembl
chr4:21414430..21508604hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3894175
hg1994175
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367170
Supporting Variants
Samples
Known GenesKCNIP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212859
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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