A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045666



Internal ID21954930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:107761629..107761629hg38UCSC Ensembl
chrX:107004859..107004859hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17646658
Samples
Known GenesTSC22D3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045666
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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