A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359152



Internal ID22246418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28880308..28880677hg38UCSC Ensembl
chr1:29206820..29207189hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38370
hg19370
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196943
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359152
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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