A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6138091



Internal ID337273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:66557304..66577214hg38UCSC Ensembl
chrX:65777146..65797056hg19UCSC Ensembl
CytobandXq12
Allele length
AssemblyAllele length
hg3819911
hg1919911
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17740438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6138091
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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