A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100799



Internal ID21504990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25033591..25033591hg38UCSC Ensembl
chr18:22613555..22613555hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38405
hg19405
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5663010
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100799
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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