A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14105097



Internal ID21276705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:139110848..139180867hg38UCSC Ensembl
InnerchrX:138193010..138263029hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3870020
hg1970020
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111703
Supporting Variants
Samplessample240
Known GenesFGF13
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14105097
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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