A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101842



Internal ID21287779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:56713632..56734216hg38UCSC Ensembl
InnerchrX:56740065..56760649hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3820585
hg1920585
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111064
Supporting Variants
Samplessample407
Known GenesLOC550643
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101842
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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