A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194030



Internal ID22344401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78805275..78805340hg38UCSC Ensembl
chr11:78516320..78516385hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14443793, nssv14379410, nssv14415484
SamplesNA19240, HG00733, HG00514
Known GenesTENM4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3194030
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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