A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659552



Internal ID21607857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:95245208..95245208hg38UCSC Ensembl
chr14:95711545..95711545hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17085854
SamplesNA12329
Known GenesCLMN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659552
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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