A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106743



Internal ID22015976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:22055060..22055118hg38UCSC Ensembl
chrX:22073178..22073236hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17644686
Samples
Known GenesPHEX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106743
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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