A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14281676



Internal ID22139457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:40514133..40614069hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3899937
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229144
Supporting Variants
SamplesHG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14281676
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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