A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987266



Internal ID21896609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:172413325..172414679hg38UCSC Ensembl
chr2:173278053..173279407hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532805
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987266
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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