A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416098



Internal ID195336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:141105000..141113500hg38UCSC Ensembl
chrX:140199174..140207685hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg388501
hg198512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742720
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416098
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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