A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099150



Internal ID21471084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34374247..34374247hg38UCSC Ensembl
chr14:34843453..34843453hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5658707
Supporting Variants
SamplesHG03125
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099150
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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