A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14391334



Internal ID22306423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62143052..62143258hg38UCSC Ensembl
chr11:61910524..61910730hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3195966
Supporting Variants
SamplesNA19240
Known GenesINCENP
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14391334
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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