A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17120284



Internal ID21448878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42008088..42008088hg38UCSC Ensembl
chr22:42404092..42404092hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667610
Supporting Variants
SamplesHG00864
Known GenesWBP2NL
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17120284
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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