A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101084



Internal ID21505031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:24489622..24489622hg38UCSC Ensembl
chr18:22069586..22069586hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5656151
Supporting Variants
SamplesNA19650
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101084
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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