A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5840167



Internal ID22615102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:88548277..88585952hg38UCSC Ensembl
chr4:89469428..89507103hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3837676
hg1937676
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17497943
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5840167
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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