A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104059



Internal ID21280603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135643179..135697986hg38UCSC Ensembl
InnerchrX:134777104..134831701hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3854808
hg1954598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118045
Supporting Variants
Samplessample30
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104059
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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