A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659209



Internal ID21607514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95259980..95259980hg38UCSC Ensembl
chr14:95726317..95726317hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg381496
hg191496
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084239
SamplesHG02587
Known GenesCLMN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659209
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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