A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211150



Internal ID22358806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62816624..62816732hg38UCSC Ensembl
chr20:61447976..61448084hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299745, nssv14299746
SamplesHG00731, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211150
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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