A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17072356



Internal ID21437165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10802029..10802029hg38UCSC Ensembl
chr11:10823576..10823576hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656224
Supporting Variants
SamplesHG00731
Known GenesEIF4G2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17072356
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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