A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656386



Internal ID21604691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51741895..51741895hg38UCSC Ensembl
chr14:52208613..52208613hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17098574
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656386
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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