A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14442787



Internal ID22238991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:15890980..15891069hg38UCSC Ensembl
chr11:15912526..15912615hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3201363
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)nssv14442787
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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