A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17125615



Internal ID21497304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120442807..120446103hg38UCSC Ensembl
chr3:120161654..120164950hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg383297
hg193297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5571180
Supporting Variants
SamplesNA19238
Known GenesFSTL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17125615
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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