A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14389877



Internal ID22211069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89776212..89776324hg38UCSC Ensembl
chr1:90241771..90241883hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3205377
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14389877
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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