A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6137915



Internal ID337096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20223456..20223545hg38UCSC Ensembl
chrX:20241574..20241663hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17739558
Samples
Known GenesRPS6KA3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6137915
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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