A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900936



Internal ID22676083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:94158443..94158536hg38UCSC Ensembl
chr4:95079594..95079687hg19UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428668
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900936
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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