A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840027



Internal ID22614962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6622443..6624942hg38UCSC Ensembl
chr4:6624170..6626669hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497117
Samples
Known GenesMAN2B2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840027
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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