A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228156



Internal ID22370430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:23291523..23432978hg38UCSC Ensembl
Outerchr15:23564854..23678125hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38141456
hg19113272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14258508
SamplesHG00732
Known GenesGOLGA8S, LOC440243
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228156
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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