A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889257



Internal ID22664273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:175019040..175020085hg38UCSC Ensembl
chr4:175940191..175941236hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg381046
hg191046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421038
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889257
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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