A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3233547



Internal ID22372789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58520198..58520339hg38UCSC Ensembl
chr20:57095254..57095395hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14301020, nssv14301021, nssv14301019
SamplesHG00512, HG00513, HG00514
Known GenesAPCDD1L-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3233547
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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