A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528866



Internal ID22398258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75610906..75610993hg38UCSC Ensembl
chr6:76320622..76320709hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14327905, nssv14327904, nssv14327903
SamplesHG00731, HG00732, HG00733
Known GenesSENP6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528866
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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