A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075647



Internal ID21454189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64489699..64489699hg38UCSC Ensembl
chr11:64257171..64257171hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663344
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075647
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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