A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3247629



Internal ID22376769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:42630481..42726862hg38UCSC Ensembl
Outerchr11:42652031..42748412hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg382924
hg192924
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14255696, nssv14255697
SamplesHG00512, HG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3247629
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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