A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193526



Internal ID22343961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26343597..26351342hg38UCSC Ensembl
chr6:26343825..26351570hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg387746
hg197746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7789n152
Supporting Variantsnssv14326853, nssv14326854
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193526
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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