A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3237740



Internal ID22373959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:28795363..28818825hg38UCSC Ensembl
Outerchr10:29084292..29107754hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38721
hg19721
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14253845, nssv14252732
SamplesHG00512, HG00732
Known GenesLINC00837
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3237740
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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