A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17081107



Internal ID21445307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57277715..57277715hg38UCSC Ensembl
chr14:57744433..57744433hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38278
hg19278
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662952
Supporting Variants
SamplesHG00732
Known GenesAP5M1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17081107
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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