A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357628



Internal ID22142664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33848549..33851320hg38UCSC Ensembl
chr11:33870095..33872866hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382772
hg192772
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528952
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357628
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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