A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358544



Internal ID21016097
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 StatusM
Merged Variants
Supporting Variantsnssv18209443
Samples
Known GenesFGFRL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358544
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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