A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14456685



Internal ID22250893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:36193879..36193947hg38UCSC Ensembl
chr18:33773842..33773910hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198102
Supporting Variants
SamplesHG00733
Known GenesMOCOS
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14456685
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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