A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14358792



Internal ID22196840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86247099..86252515hg38UCSC Ensembl
chr11:85958141..85963557hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg385417
hg195417
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3230273
Supporting Variants
SamplesHG00731
Known GenesEED
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14358792
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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