A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220332



Internal ID22365057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:6287224..6340790hg38UCSC Ensembl
Outerchr19:6287235..6340801hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3853567
hg1953567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14263573
SamplesNA19239
Known GenesACER1
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220332
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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