A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358241



Internal ID22257651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28250928..28251506hg38UCSC Ensembl
chr1:28577439..28578017hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3191053
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358241
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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