A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114100



Internal ID21297366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:124997222..125015915hg38UCSC Ensembl
InnerchrX:124131071..124149764hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3818694
hg1918694
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104950
Samplessample137
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114100
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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