A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987753



Internal ID21897096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231697391..231697478hg38UCSC Ensembl
chr2:232562101..232562188hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987753
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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