A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221501



Internal ID22365871
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14278159, nssv14278160
SamplesNA19239, NA19240
Known GenesMPP7
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221501
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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