A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3208963



Internal ID22357112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99823164..99829853hg38UCSC Ensembl
chr6:100271040..100277729hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg386690
hg196690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14328822
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3208963
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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