A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14332139



Internal ID22182946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166221911..166221978hg38UCSC Ensembl
chr6:166635399..166635466hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207625
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14332139
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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