A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5850809



Internal ID22625744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:79421994..79423378hg38UCSC Ensembl
chr11:79133038..79134422hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381385
hg191385
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465548
Samples
Known GenesMIR5579, TENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5850809
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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