A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135699



Internal ID21482805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37509602..37509602hg38UCSC Ensembl
chr22:37905609..37905609hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5668291
Supporting Variants
SamplesHG03732
Known GenesCARD10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135699
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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