A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222943



Internal ID22366858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:63871889..63885628hg38UCSC Ensembl
Outerchr10:65631649..65645388hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3813740
hg1913740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14279639
SamplesHG00512
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222943
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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