A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194264



Internal ID22344599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:149309647..149354144hg38UCSC Ensembl
Outerchr4:150230799..150275296hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg3844498
hg1944498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14273061, nssv14273062
SamplesNA19238, HG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3194264
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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