A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5906211



Internal ID22681408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54986044..54989267hg38UCSC Ensembl
chr4:55852211..55855434hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg383224
hg193224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415393
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5906211
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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