A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209757



Internal ID22357785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:107578644..107655933hg38UCSC Ensembl
Outerchr3:107297491..107374780hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3877290
hg1977290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271689
SamplesNA19239
Known GenesBBX
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209757
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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