A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6059397



Internal ID21968631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103366173..103366173hg38UCSC Ensembl
chrX:102621101..102621101hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644087
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6059397
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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