A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882202



Internal ID22657179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62441635..62443623hg38UCSC Ensembl
chr17:60518996..60520984hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381989
hg191989
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475762
Samples
Known GenesMETTL2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882202
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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