A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198779



Internal ID22348465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41058278..41058407hg38UCSC Ensembl
chr6:41026017..41026146hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14326392, nssv14326393
SamplesHG00512, HG00513
Known GenesAPOBEC2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198779
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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