A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14355362



Internal ID22283243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15594012..15598679hg38UCSC Ensembl
chr11:15615558..15620225hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg384668
hg194668
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226460
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14355362
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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