A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14326851



Internal ID22323815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11000057..11002245hg38UCSC Ensembl
chr1:11060114..11062302hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382189
hg192189
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198347
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14326851
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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