A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536932



Internal ID250296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:101137985..101137985hg38UCSC Ensembl
chrX:100392974..100392974hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38672
hg19672
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17741710
Samples
Known GenesCENPI
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536932
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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