A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14357076



Internal ID22196276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69176999..69182944hg38UCSC Ensembl
chr11:68944467..68950412hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg385946
hg195946
Variant TypeOTHER sequence alteration
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3231467
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14357076
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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