A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101655



Internal ID21278943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:139929227..139934291hg38UCSC Ensembl
InnerchrX:139011386..139016450hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg385065
hg195065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110488
Supporting Variants
Samplessample275
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101655
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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