A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14437046



Internal ID22180235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11282959..11285517hg38UCSC Ensembl
chr10:11324922..11327480hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg382559
hg192559
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3203238
Supporting Variants
SamplesHG00514
Known GenesCELF2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14437046
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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