A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3286748



Internal ID22385141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19940070..19940150hg38UCSC Ensembl
chr6:19940301..19940381hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14436566
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3286748
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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