A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3229225



Internal ID22371136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:99880587..99892126hg38UCSC Ensembl
Outerchr10:101640344..101651883hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3811540
hg1911540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14277716
SamplesNA19238
Known GenesDNMBP
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3229225
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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