A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904452



Internal ID22679629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:43264795..43272510hg38UCSC Ensembl
chr4:43266812..43274527hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg387716
hg197716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904452
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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