A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14361355



Internal ID22197595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120061467..120061949hg38UCSC Ensembl
chr11:119932176..119932658hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3557710
Supporting Variants
SamplesHG00732
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14361355
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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