A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18188448



Internal ID20755488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14270527..14395207hg38UCSC Ensembl
chr18:14270526..14395206hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38124681
hg19124681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523440
Supporting Variants
Samples
Known GenesCYP4F35P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18188448
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00116


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