A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14275342



Internal ID22261864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:65687971..65738674hg38UCSC Ensembl
Outerchr10:67447729..67498432hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3850704
hg1950704
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211632
Supporting Variants
SamplesNA19238
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14275342
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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