A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14396437



Internal ID22302153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44539672..44539672hg38UCSC Ensembl
chr22:44935552..44935552hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3557040
Supporting Variants
SamplesNA19240
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)nssv14396437
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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