A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643474



Internal ID21591779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110185397..110185397hg38UCSC Ensembl
chr6:110506600..110506600hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38195
hg19195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17151166
SamplesHG03486
Known GenesCDC40
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643474
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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