A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207655



Internal ID22356013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100932233..100937065hg38UCSC Ensembl
chr6:101380109..101384941hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg384833
hg194833
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8032n152
Supporting Variantsnssv14328844, nssv14328845
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207655
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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