A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14258770



Internal ID22253370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:58470834..58496016hg38UCSC Ensembl
Outerchr15:58763033..58788215hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3825183
hg1925183
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3228669
Supporting Variants
SamplesNA19238
Known GenesLIPC
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14258770
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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