A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138507



Internal ID337691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55728000..56175100hg38UCSC Ensembl
chrX:55754433..56201533hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38447101
hg19447101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740215
Samples
Known GenesRRAGB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138507
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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