A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564370



Internal ID22433101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42408267..42408267hg38UCSC Ensembl
chr6:42376005..42376005hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14326458
SamplesHG00513
Known GenesTRERF1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564370
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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