A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528709



Internal ID22398099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131363266..131363337hg38UCSC Ensembl
chr6:131684406..131684477hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330983, nssv14330984
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528709
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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