A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749981



Internal ID20526016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39898253..39898315hg38UCSC Ensembl
chr8:39755772..39755834hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273112
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749981
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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