A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101840



Internal ID21287782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:56238080..56422579hg38UCSC Ensembl
InnerchrX:56264513..56449012hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg38184500
hg19184500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110385
Supporting Variants
Samplessample407
Known GenesKLF8
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101840
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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