A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355471



Internal ID22180192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18528045..18528376hg38UCSC Ensembl
chr11:18549592..18549923hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221768
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355471
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer