A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636254



Internal ID21584559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:113240143..113240143hg38UCSC Ensembl
chr6:113561345..113561345hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17145611
SamplesHG03371
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636254
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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