A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14275598



Internal ID22153589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:111899278..111908692hg38UCSC Ensembl
Outerchr6:112220481..112229895hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg389415
hg199415
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208198
Supporting Variants
SamplesHG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14275598
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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