A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5633708



Internal ID21582013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:113444216..113444216hg38UCSC Ensembl
chr8:114456445..114456445hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17157777
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5633708
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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