A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6109132



Internal ID22018365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:109556729..109556890hg38UCSC Ensembl
chrX:108799958..108800119hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6109132
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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