A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114644



Internal ID21297910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:95058165..95124727hg38UCSC Ensembl
InnerchrX:94313164..94379726hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3866563
hg1966563
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104079, nssv14105085, nssv14104114
Samplessample60, sample231, sample46
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114644
Frequency
Sample Size467
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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