A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903698



Internal ID22678867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207624402..207625058hg38UCSC Ensembl
chr2:208489126..208489782hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401796
Samples
Known GenesMETTL21A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903698
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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