A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528627



Internal ID18480222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37087152..37194938hg38UCSC Ensembl
Innerchr14:37556357..37664143hg19UCSC Ensembl
Innerchr14:36626108..36733894hg18UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38107787
hg19107787
hg18107787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050174
Supporting Variants
Samples
Known GenesSLC25A21, SLC25A21-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3528627
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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