A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114800



Internal ID21298066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7338596..7359106hg38UCSC Ensembl
InnerchrX:7256637..7277147hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3820511
hg1920511
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104093
Samplessample53
Known GenesSTS
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114800
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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