A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14275988



Internal ID22261012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:141709797..141742355hg38UCSC Ensembl
Outerchr6:142030934..142063492hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3832559
hg1932559
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3208476
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14275988
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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