A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3206965



Internal ID22355435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137061103..137061427hg38UCSC Ensembl
chr6:137382240..137382564hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330295
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3206965
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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