A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101997



Internal ID21493401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75165424..75165535hg38UCSC Ensembl
chr18:72877379..72877490hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598139
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101997
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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