A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903590



Internal ID22678759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183886056..183886107hg38UCSC Ensembl
chr4:184807209..184807260hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17416168
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903590
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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