A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115773



Internal ID21299039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:38527502..38539809hg38UCSC Ensembl
InnerchrX:38386755..38399062hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3812308
hg1912308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104108
Samplessample56
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115773
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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