A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047241



Internal ID21956474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:130466441..130466441hg38UCSC Ensembl
chrX:129600415..129600415hg19UCSC Ensembl
CytobandXq26.1
Allele length
AssemblyAllele length
hg382073
hg192073
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647099
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047241
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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