A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096439



Internal ID21507370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:97787606..97787606hg38UCSC Ensembl
chr14:98253943..98253943hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381029
hg191029
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651125
Supporting Variants
SamplesNA19983
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096439
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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