A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111426



Internal ID21294692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:144530683..144865323hg38UCSC Ensembl
InnerchrX:143612204..143946844hg19UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38334641
hg19334641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101639
Samplessample268
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111426
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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