A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893996



Internal ID22669064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:66108683..66111043hg38UCSC Ensembl
chr4:66974401..66976761hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg382361
hg192361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17410258
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893996
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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