A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14360537



Internal ID22129460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67414288..67414778hg38UCSC Ensembl
chr11:67181759..67182249hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529997
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14360537
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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