A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104118



Internal ID21290695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87160443..87198501hg38UCSC Ensembl
InnerchrX:86415446..86453504hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3838059
hg1938059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117522
Supporting Variants
Samplessample62
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104118
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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