A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213024



Internal ID22360101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:13897724..13938362hg38UCSC Ensembl
Outerchr9:13897723..13938361hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg3840639
hg1940639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14282913
SamplesHG00732
Known GenesLINC00583
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213024
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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