A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643983



Internal ID21592288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37734478..37734478hg38UCSC Ensembl
chr8:37591996..37591996hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17140646
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643983
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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