A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624859



Internal ID21573164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45904647..45904647hg38UCSC Ensembl
chr6:45872384..45872384hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17150171, nssv17144390
SamplesHG00731, HG00732
Known GenesCLIC5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624859
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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