A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104936



Internal ID21268176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:110080448..110090643hg38UCSC Ensembl
InnerchrX:109323676..109333871hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3810196
hg1910196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112458
Supporting Variants
Samplessample121
Known GenesMIR3978, TMEM164
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104936
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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