A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14443885



Internal ID22239940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:134138440..134138513hg38UCSC Ensembl
chr11:134008335..134008408hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3195345
Supporting Variants
SamplesHG00733
Known GenesJAM3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14443885
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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