A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101140



Internal ID21405148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:34166741..34167077hg38UCSC Ensembl
chr18:31746705..31747041hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586324
Supporting Variants
SamplesHG00512
Known GenesNOL4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101140
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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