A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5416867



Internal ID196079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:36578745..36841831hg38UCSC Ensembl
chrX:36596819..36859904hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38263087
hg19263086
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5416867
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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