A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14253397



Internal ID22230847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:63770580..63826436hg38UCSC Ensembl
Outerchr10:65530340..65586196hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381283
hg191283
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3250109
Supporting Variants
SamplesHG00733
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14253397
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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