A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17075789



Internal ID21415468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69482419..69482419hg38UCSC Ensembl
chr11:69297187..69297187hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649654
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17075789
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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