A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5595491



Internal ID21544097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:39510776..39510871hg38UCSC Ensembl
chr22:39906781..39906876hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137466
SamplesHG02587
Known GenesMIEF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5595491
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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