A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5636360



Internal ID21584665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:112573215..112573215hg38UCSC Ensembl
chr6:112894417..112894417hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157254
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5636360
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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