A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052689



Internal ID21961922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:144373378..144373378hg38UCSC Ensembl
chrX:143456471..143456471hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17643404
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052689
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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