A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032263



Internal ID21941606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62445520..62451622hg38UCSC Ensembl
chr17:60522881..60528983hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg386103
hg196103
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17625438
Samples
Known GenesMETTL2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032263
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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