A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5844304



Internal ID22619239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110243457..110248513hg38UCSC Ensembl
chr6:110564660..110569716hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385057
hg195057
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17500914
Samples
Known GenesMETTL24
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5844304
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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