A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102539



Internal ID21289271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:14951112..15128639hg38UCSC Ensembl
Innerchr1:15277608..15455135hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38177528
hg19177528
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117133
Supporting Variants
Samplessample45
Known GenesKAZN, TMEM51-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102539
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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