A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207638



Internal ID22355996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44510750..44510803hg38UCSC Ensembl
chr3:44552242..44552295hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5952n152
Supporting Variantsnssv14306833, nssv14306832
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207638
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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