A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228917



Internal ID22370940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:96000098..96018448hg38UCSC Ensembl
Outerchr3:95718942..95737292hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38776
hg19776
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14272216
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228917
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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