A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740824



Internal ID20516801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:41626334..41626437hg38UCSC Ensembl
chr8:41483853..41483956hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16291677
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740824
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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