A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5608798



Internal ID21557103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10631054..10631054hg38UCSC Ensembl
chr4:10632678..10632678hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386076
hg196076
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17120672
SamplesNA24385
Known GenesCLNK
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5608798
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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