A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3114278



Internal ID21297544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:56402558..56422579hg38UCSC Ensembl
InnerchrX:56428991..56449012hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3820022
hg1920022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104146
Samplessample85
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3114278
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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