A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5904024



Internal ID22679197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185128077..185129616hg38UCSC Ensembl
chr4:186049231..186050770hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381540
hg191540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1614n209
Supporting Variantsnssv17410213
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5904024
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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