A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14447476



Internal ID22243069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62443524..62443632hg38UCSC Ensembl
chr18:60110757..60110865hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3192142
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)nssv14447476
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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