A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749887



Internal ID20525922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37572184..37572244hg38UCSC Ensembl
chr20:36200586..36200646hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16292266
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749887
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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