A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050174



Internal ID18792705
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 StatusM
Merged Variantsdgv1871n100
Supporting Variantsnssv3528627
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)nsv1050174
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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