A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360071



Internal ID22211439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93866427..93866502hg38UCSC Ensembl
chr11:93599593..93599668hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529545
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360071
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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