A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5966028



Internal ID22740963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:47626314..47626363hg38UCSC Ensembl
chr22:48022063..48022112hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17400400
Samples
Known GenesLINC00898
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5966028
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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