A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110281



Internal ID22019514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:111795903..111796011hg38UCSC Ensembl
chrX:111039131..111039239hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648685
Samples
Known GenesTRPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110281
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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