A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5889893



Internal ID22664915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102210708..102248570hg38UCSC Ensembl
chr4:103131865..103169727hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3837863
hg1937863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17421751
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5889893
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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