A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3190477



Internal ID22341333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:137299645..137326204hg38UCSC Ensembl
Outerchr3:137018487..137045046hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3826560
hg1926560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14271709
SamplesNA19239
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3190477
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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