A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102106



Internal ID22011340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154090218..154090328hg38UCSC Ensembl
chrX:153355676..153355786hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638492
Samples
Known GenesMECP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102106
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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