A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644662



Internal ID21592967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:106910640..106910640hg38UCSC Ensembl
chr13:107562988..107562988hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097127
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644662
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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