A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107581



Internal ID22016814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154090217..154090442hg38UCSC Ensembl
chrX:153355675..153355900hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645409
Samples
Known GenesMECP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107581
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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