A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14254080



Internal ID22254750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:24300608..24374923hg38UCSC Ensembl
Outerchr11:24322154..24396469hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg386445
hg196445
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3244764
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14254080
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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