A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358886



Internal ID22245512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57403445..57403445hg38UCSC Ensembl
chr11:57170918..57170918hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3559562
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358886
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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