A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938015



Internal ID22713391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62447169..62462823hg38UCSC Ensembl
chr17:60524530..60540184hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg3815655
hg1915655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373068
Samples
Known GenesMETTL2A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938015
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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