A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730543



Internal ID20506455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:36976351..36976529hg38UCSC Ensembl
chr20:35604754..35604932hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38179
hg19179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264717
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4730543
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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