A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5890886



Internal ID22665916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86931761..86932071hg38UCSC Ensembl
chr4:87852913..87853223hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17429021
Samples
Known GenesLOC100506746
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5890886
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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