A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14087977



Internal ID21278901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105240949..105246913hg38UCSC Ensembl
Innerchr9:108003230..108009194hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385965
hg195965
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111597
Supporting Variants
Samplessample275
Known GenesSLC44A1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14087977
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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