A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14101637



Internal ID21278376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:108777609..108840400hg38UCSC Ensembl
InnerchrX:108020839..108083630hg19UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3862792
hg1962792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117281
Supporting Variants
Samplessample268
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14101637
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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