A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902760



Internal ID22677921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107419594..107419649hg38UCSC Ensembl
chr4:108340751..108340806hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17422827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902760
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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