A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6089878



Internal ID21999111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77705047..77705047hg38UCSC Ensembl
chr13:78279182..78279182hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17601453
Samples
Known GenesSLAIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6089878
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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