A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135220



Internal ID21461930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:31269916..31269977hg38UCSC Ensembl
chr22:31665902..31665963hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599238
Supporting Variants
SamplesHG02818
Known GenesLIMK2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135220
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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