A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17100786



Internal ID21472665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21757371..21757470hg38UCSC Ensembl
chr18:19337332..19337431hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603515
Supporting Variants
SamplesHG03371
Known GenesMIB1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17100786
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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