A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224857



Internal ID22368166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:67544281..67560275hg38UCSC Ensembl
Outerchr9:38804014..38820017hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3815995
hg1916004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282899
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224857
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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