A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116878



Internal ID21300144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:34877993..34970057hg38UCSC Ensembl
InnerchrX:34896110..34988174hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3892065
hg1992065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104994
Samplessample163
Known GenesFAM47B
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116878
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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