A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14299838



Internal ID22203098
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3535071
Supporting Variants
SamplesHG00732
Known GenesASXL1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14299838
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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