A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112661



Internal ID21295927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:10713748..10730503hg38UCSC Ensembl
InnerchrX:10681788..10698543hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3816756
hg1916756
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104034, nssv14104185
Samplessample11, sample116
Known GenesMID1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112661
Frequency
Sample Size467
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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