A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211801



Internal ID22359243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:57833771..57833982hg38UCSC Ensembl
chr20:56408827..56409038hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14300390, nssv14301006, nssv14300389
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211801
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer