A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139028



Internal ID338212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153595643..153597060hg38UCSC Ensembl
chrX:152861101..152862518hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381418
hg191418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17738081
Samples
Known GenesFAM58A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139028
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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