A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201864



Internal ID22351107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:67593226..67593354hg38UCSC Ensembl
chr3:67643650..67643778hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307388, nssv14307389
SamplesNA19238, NA19240
Known GenesSUCLG2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201864
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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