A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215124



Internal ID22361559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:115482160..115540541hg38UCSC Ensembl
Outerchr10:117241670..117300051hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3858382
hg1958382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14279857
SamplesHG00731
Known GenesATRNL1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215124
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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