A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14258419



Internal ID22320301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:95340201..95357237hg38UCSC Ensembl
Outerchr15:95883430..95900466hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg3817037
hg1917037
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222349
Supporting Variants
SamplesNA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14258419
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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