A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3232978



Internal ID22372641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:9362348..9365069hg38UCSC Ensembl
Outerchr10:9404311..9407032hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38162481
hg19162481
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253470
SamplesHG00514
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3232978
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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