A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903637



Internal ID22678806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26045317..26056880hg38UCSC Ensembl
chr4:26046939..26058502hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3811564
hg1911564
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903637
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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