A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14446103



Internal ID22241878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26784428..26784567hg38UCSC Ensembl
chr18:24364392..24364531hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204697
Supporting Variants
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)nssv14446103
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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