A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104115



Internal ID21290629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:76789144..76893177hg38UCSC Ensembl
InnerchrX:76009569..76113602hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38104034
hg19104034
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112225
Supporting Variants
Samplessample61
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104115
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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