A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14281642



Internal ID22254717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:28063112..28089005hg38UCSC Ensembl
Outerchr9:28063110..28089003hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3825894
hg1925894
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221483
Supporting Variants
SamplesNA19238
Known GenesLINGO2
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14281642
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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