A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3197259



Internal ID22347162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70662441..70783023hg38UCSC Ensembl
chr3:70711592..70832174hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38120583
hg19120583
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14305502
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3197259
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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