A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4745078



Internal ID20521083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214864035..214866104hg38UCSC Ensembl
chr2:215728759..215730828hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg382070
hg192070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266106
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4745078
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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