A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14352991



Internal ID22233185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:20381552..20382469hg38UCSC Ensembl
chr1:20708045..20708962hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207014
Supporting Variants
SamplesHG00733
Known GenesLINC01141
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14352991
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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