A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101844



Internal ID21287846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:65369839..65372253hg38UCSC Ensembl
InnerchrX:64589719..64592133hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg382415
hg192415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117688
Supporting Variants
Samplessample408
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101844
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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