A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3203395



Internal ID22352413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69106861..69107454hg38UCSC Ensembl
chr3:69156012..69156605hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307453, nssv14307454
SamplesNA19238, NA19239
Known GenesLMOD3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3203395
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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