A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219587



Internal ID22364567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32832656..32832831hg38UCSC Ensembl
chr20:31420462..31420637hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299856
SamplesHG00731
Known GenesMAPRE1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219587
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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