A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14359812



Internal ID22253866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64168997..64169594hg38UCSC Ensembl
chr11:63936469..63937066hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217864
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14359812
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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