A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742679



Internal ID20518664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56175336..56179838hg38UCSC Ensembl
chr20:54750392..54754894hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384503
hg194503
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16287529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742679
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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