A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103104



Internal ID21499248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9877538..9877909hg38UCSC Ensembl
chr18:9877535..9877906hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5587424
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103104
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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