A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14276333



Internal ID22198629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:91858398..91862379hg38UCSC Ensembl
Outerchr5:91154215..91158196hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3845548
hg1945548
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226028
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14276333
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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