A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641231



Internal ID21589536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27380362..27380362hg38UCSC Ensembl
chr6:27348141..27348141hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17141592
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641231
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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