A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105045



Internal ID21274169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:128920414..129044170hg38UCSC Ensembl
InnerchrX:128054392..128178147hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38123757
hg19123756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118140
Supporting Variants
Samplessample202
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105045
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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