A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14414782



Internal ID22150240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:42721627..42722650hg38UCSC Ensembl
chr11:42743177..42744200hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381024
hg191024
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202368
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14414782
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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