A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201327



Internal ID22350655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41586851..41599300hg38UCSC Ensembl
chr6:41554589..41567038hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3812450
hg1912450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14326429, nssv14326427, nssv14326428, nssv14326430, nssv14326432, nssv14326426, nssv14326431, nssv14326425, nssv14326424
SamplesHG00512, NA19238, NA19239, HG00731, HG00732, NA19240, HG00733, HG00513, HG00514
Known GenesFOXP4, MIR4641
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201327
Frequency
Sample Size9
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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