A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202917



Internal ID22352011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34093225..34098991hg38UCSC Ensembl
chr3:34134717..34140483hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385767
hg195767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307998, nssv14307999
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202917
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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