A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3115879



Internal ID21299145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:85384631..85385847hg38UCSC Ensembl
InnerchrX:84639636..84640852hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14101812
Samplessample394
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3115879
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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