A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14258461



Internal ID22201121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:98262964..98303123hg38UCSC Ensembl
Outerchr15:98806193..98846352hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3840160
hg1940160
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3218488
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14258461
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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