A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115046



Internal ID21298312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:29582027..29590784hg38UCSC Ensembl
InnerchrX:29600144..29608901hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg388758
hg198758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1261n145
Supporting Variantsnssv14105109
Samplessample249
Known GenesIL1RAPL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115046
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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