A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14414266



Internal ID22149660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118012618..118012668hg38UCSC Ensembl
chr10:119772129..119772179hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206638
Supporting Variants
SamplesHG00514
Known GenesRAB11FIP2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14414266
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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