A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5418695



Internal ID197857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:103898344..103923488hg38UCSC Ensembl
chrX:103153265..103178069hg19UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg3825145
hg1924805
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737135
Samples
Known GenesMIR1256
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5418695
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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