A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17142116



Internal ID21467505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92576378..92576378hg38UCSC Ensembl
chr7:92205692..92205692hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5633171
Supporting Variants
SamplesHG03065
Known GenesFAM133B, FAM133DP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17142116
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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