A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17103079



Internal ID21428158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9385393..9385716hg38UCSC Ensembl
chr18:9385391..9385714hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595123
Supporting Variants
SamplesHG00731
Known GenesTWSG1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17103079
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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