A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526241



Internal ID22395621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1026082..1026310hg38UCSC Ensembl
chr4:1019870..1020098hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38229
hg19229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14311259, nssv14311256, nssv14311255, nssv14311257, nssv14311258
SamplesNA19238, NA19239, HG00732, NA19240, HG00733
Known GenesFGFRL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526241
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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