A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5843980



Internal ID22618915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10749734..10754378hg38UCSC Ensembl
chr6:10749967..10754611hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg384645
hg194645
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17501053, nssv17500884
Samples
Known GenesTMEM14B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5843980
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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