A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110320



Internal ID22019553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:49256207..49256263hg38UCSC Ensembl
chrX:49112668..49112720hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3857
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648553
Samples
Known GenesFOXP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110320
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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