A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17101836



Internal ID21489666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55595543..55596088hg38UCSC Ensembl
chr18:53262774..53263319hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586701
Supporting Variants
SamplesNA18939
Known GenesTCF4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17101836
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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