A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5663679



Internal ID21611984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:36810878..36810878hg38UCSC Ensembl
chr14:37280083..37280083hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17093193, nssv17084792, nssv17083189
SamplesHG03065, NA19239, HG00732
Known GenesSLC25A21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5663679
Frequency
Sample Size35
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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