A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056670



Internal ID21965903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:74435530..74435530hg38UCSC Ensembl
chrX:73655365..73655365hg19UCSC Ensembl
CytobandXq13.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647580
Samples
Known GenesSLC16A2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056670
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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