A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075645



Internal ID21455842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64366904..64366904hg38UCSC Ensembl
chr11:64134376..64134376hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381495
hg191495
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653393
Supporting Variants
SamplesHG02492
Known GenesRPS6KA4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075645
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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