A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5415654



Internal ID194907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103920542..103959771hg38UCSC Ensembl
chrX:103175125..103214344hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3839230
hg1939220
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737138
Samples
Known GenesMIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5415654
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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