A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067493



Internal ID21461899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:10787..10787hg38UCSC Ensembl
chr18:11140..11140hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5635382
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067493
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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