A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3539032



Internal ID22408203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:19003194..19003276hg38UCSC Ensembl
chr20:18983838..18983920hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5191n152
Supporting Variantsnssv14297563, nssv14297562
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3539032
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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