A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097566



Internal ID21461212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24696638..24696638hg38UCSC Ensembl
chr14:25165844..25165844hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648134
Supporting Variants
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097566
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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