A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101312



Internal ID21481152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:54342407..54344598hg38UCSC Ensembl
chr18:51868777..51870968hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg382192
hg192192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589524
Supporting Variants
SamplesHG03683
Known GenesSTARD6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101312
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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