A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358092



Internal ID22242791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7135332..7135332hg38UCSC Ensembl
chr11:7156563..7156563hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559804
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358092
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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