A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925421



Internal ID22700648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110196913..110199881hg38UCSC Ensembl
chr8:111209142..111212110hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg382969
hg192969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17441072
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925421
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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