A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670968



Internal ID21619273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48872644..48872644hg38UCSC Ensembl
chr22:49268456..49268456hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17139184
SamplesHG00171
Known GenesLOC100128946
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670968
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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