A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735572



Internal ID20511516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38010446..38014955hg38UCSC Ensembl
chr8:37867964..37872473hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg384510
hg194510
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16286031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735572
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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