A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214178



Internal ID22360904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62971712..62972277hg38UCSC Ensembl
chr20:61603064..61603629hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299759
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214178
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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