A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17141909



Internal ID21483218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39829825..39829825hg38UCSC Ensembl
chr7:39869424..39869424hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5629549
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17141909
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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