A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202586



Internal ID22351729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:154548821..154550886hg38UCSC Ensembl
chr4:155469973..155472038hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg382066
hg192066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14319047, nssv14319045, nssv14319040, nssv14319043, nssv14319041, nssv14319042, nssv14319039, nssv14319046, nssv14319044
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesPLRG1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202586
Frequency
Sample Size9
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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