A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564372



Internal ID22433103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45884971..45884971hg38UCSC Ensembl
chr6:45852708..45852708hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327233, nssv14327237, nssv14327234, nssv14327235, nssv14327236
SamplesNA19238, NA19239, HG00731, HG00732, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564372
Frequency
Sample Size9
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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