A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528566



Internal ID22397954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66025364..66025791hg38UCSC Ensembl
chr7:65490351..65490778hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335715, nssv14335716
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528566
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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