A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14255183



Internal ID22255154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:92242384..92264662hg38UCSC Ensembl
Outerchr12:92636160..92658438hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3822279
hg1922279
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218889
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14255183
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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