A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192239



Internal ID20759279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14259301..14443500hg38UCSC Ensembl
chr18:14259300..14443499hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38184200
hg19184200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6533388
Supporting Variants
Samples
Known GenesCYP4F35P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192239
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00088


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