A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095060



Internal ID21431071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:98330523..98330523hg38UCSC Ensembl
chr14:98796860..98796860hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654313
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095060
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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