A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630926



Internal ID21579231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1382032..1382032hg38UCSC Ensembl
chr6:1382267..1382267hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17143650
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630926
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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