A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209443



Internal ID20776483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1026082..1026287hg38UCSC Ensembl
chr4:1019870..1020075hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358544
Supporting Variants
Samples
Known GenesFGFRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209443
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00151


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