A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17121297



Internal ID21489378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118890546..118890618hg38UCSC Ensembl
chr4:119811701..119811773hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5566858
Supporting Variants
SamplesNA18939
Known GenesSYNPO2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17121297
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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