A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3224016



Internal ID22367594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:8261764..8300709hg38UCSC Ensembl
Outerchr10:8303727..8342672hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3838946
hg1938946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14279972
SamplesHG00732
Known GenesLINC00708
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3224016
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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