A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211883



Internal ID20778923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4918972..5083515hg38UCSC Ensembl
chr4:4920699..5085242hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38164544
hg19164544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362476
Supporting Variants
Samples
Known GenesCYTL1, STK32B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211883
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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