A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112063



Internal ID21295329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:11428850..11430428hg38UCSC Ensembl
InnerchrX:11446970..11448548hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg381579
hg191579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1258n145
Supporting Variantsnssv14104062
Samplessample34
Known GenesARHGAP6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112063
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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