A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3564698



Internal ID22433428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91679325..91679325hg38UCSC Ensembl
chr6:92389043..92389043hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327347, nssv14327346
SamplesNA19239, NA19240
Known GenesCASC6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3564698
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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