A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138274



Internal ID337458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:113972597..113981006hg38UCSC Ensembl
chrX:113215858..113224247hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg388410
hg198390
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17742078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138274
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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