A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626286



Internal ID21574591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2797854..2797854hg38UCSC Ensembl
chr6:2798088..2798088hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143864
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626286
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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