A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5427333



Internal ID206238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:15782749..15782879hg38UCSC Ensembl
chrX:15800872..15801002hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739408
Samples
Known GenesCA5B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5427333
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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