A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14386476



Internal ID22302858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75763434..75763746hg38UCSC Ensembl
chr11:75474479..75474791hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202995
Supporting Variants
SamplesNA19240
Known GenesLOC283214
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14386476
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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