A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17074490



Internal ID21508405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22637441..22637441hg38UCSC Ensembl
chr11:22658987..22658987hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656230
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17074490
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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