A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195751



Internal ID22345882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:180860113..180860257hg38UCSC Ensembl
chr3:180577901..180578045hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310096, nssv14310097
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195751
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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