A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112833



Internal ID21296099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:98987799..99023714hg38UCSC Ensembl
InnerchrX:98242797..98278712hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3835916
hg1935916
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14104057
Samplessample29
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112833
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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