A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564605



Internal ID22433335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69122018..69122018hg38UCSC Ensembl
chr6:69831910..69831910hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14328585, nssv14328582, nssv14328583, nssv14328584
SamplesHG00731, HG00732, HG00733, HG00513
Known GenesBAI3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564605
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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