A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894074



Internal ID22669143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170219186..170219372hg38UCSC Ensembl
chr4:171140337..171140523hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894074
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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