A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3228633



Internal ID22370756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18234674..18875793hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38641120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5671n152
Supporting Variantsnssv14461039
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3228633
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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