A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528026



Internal ID22397412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107149409..107149606hg38UCSC Ensembl
chr6:107470613..107470810hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330771, nssv14330770, nssv14330769, nssv14330772
SamplesNA19238, HG00732, NA19240, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528026
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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