A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112621



Internal ID21295887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:115684951..115690053hg38UCSC Ensembl
InnerchrX:114919271..114924373hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385103
hg195103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105114
Samplessample254
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112621
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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