A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104047



Internal ID21273291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:9141765..9151542hg38UCSC Ensembl
InnerchrX:9109806..9119583hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg389778
hg199778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110379
Supporting Variants
Samplessample19
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104047
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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