A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639564



Internal ID21587869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5480009..5480009hg38UCSC Ensembl
chr10:5521972..5521972hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070717
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639564
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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