A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215101



Internal ID22361543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:24624185..24685779hg38UCSC Ensembl
Outerchr9:24624183..24685777hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3861595
hg1961595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282842, nssv14282915
SamplesHG00732, HG00513
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215101
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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