A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17073473



Internal ID21489986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127942193..127942193hg38UCSC Ensembl
chr11:127812088..127812088hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655423
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17073473
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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