A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3535071



Internal ID22404331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:32377022..32377207hg38UCSC Ensembl
chr20:30964825..30965010hg19UCSC Ensembl
Cytoband20q11.21
Allele length
AssemblyAllele length
hg38186
hg19186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14299840, nssv14299838, nssv14299839, nssv14299837, nssv14299836
SamplesNA19239, HG00732, HG00733, HG00513, HG00514
Known GenesASXL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3535071
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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