A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207014



Internal ID22355479
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352991
SamplesHG00733
Known GenesLINC01141
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207014
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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