A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14380805



Internal ID22290889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:37940643..37940970hg38UCSC Ensembl
chr11:37962193..37962520hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3204976
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14380805
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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