A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209732



Internal ID22357762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:196525761..196534984hg38UCSC Ensembl
Outerchr3:196252632..196261855hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg389224
hg199224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14270897
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209732
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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