A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189807



Internal ID20756847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:37568301..37643600hg38UCSC Ensembl
chr14:38037506..38112805hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3875300
hg1975300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494024
Supporting Variants
Samples
Known GenesFOXA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189807
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00089


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