A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086105



Internal ID21476107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102677289..102677289hg38UCSC Ensembl
chr14:103143626..103143626hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5653908
Supporting Variants
SamplesHG03486
Known GenesRCOR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086105
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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