A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106298



Internal ID22015531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120279938..120279999hg38UCSC Ensembl
chrX:119413793..119413854hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648873
Samples
Known GenesTMEM255A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106298
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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