A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14278159



Internal ID22277916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:28211867..28230395hg38UCSC Ensembl
Outerchr10:28500796..28519324hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3818529
hg1918529
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221501
Supporting Variants
SamplesNA19239
Known GenesMPP7
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14278159
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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