A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222970



Internal ID22366873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:84393091..84432121hg38UCSC Ensembl
Outerchr15:84947789..84984473hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3839031
hg1936685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258838, nssv14258839
SamplesNA19238, HG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222970
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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