A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638798



Internal ID21587103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27842919..27842919hg38UCSC Ensembl
chr6:27810697..27810697hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151745
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638798
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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