A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748990



Internal ID20525018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:98956516..98956569hg38UCSC Ensembl
chr8:99968744..99968797hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16289492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748990
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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