A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893492



Internal ID22668552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:108084185..108084274hg38UCSC Ensembl
chr3:107803032..107803121hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17405555
Samples
Known GenesCD47
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893492
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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