A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14096249



Internal ID21273374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57583974..57612826hg38UCSC Ensembl
Innerchr15:57876172..57905024hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3828853
hg1928853
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114739
Supporting Variants
Samplessample190
Known GenesGCOM1, MYZAP
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14096249
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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