A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201702



Internal ID22350966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:158290422..158302241hg38UCSC Ensembl
Outerchr4:159211574..159223393hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3811820
hg1911820
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14275058
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201702
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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