A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14382129



Internal ID22289569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131679409..131682818hg38UCSC Ensembl
chr11:131549303..131552712hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383410
hg193410
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3198910
Supporting Variants
SamplesNA19240
Known GenesNTM
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14382129
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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