A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17076457



Internal ID21449915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96399532..96399532hg38UCSC Ensembl
chr11:96132696..96132696hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662754
Supporting Variants
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17076457
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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