A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043410



Internal ID18785941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37087152..37201854hg38UCSC Ensembl
Innerchr14:37556357..37671059hg19UCSC Ensembl
Innerchr14:36626108..36740810hg18UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg38114703
hg19114703
hg18114703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1871n100
Supporting Variantsnssv3528628
Samples
Known GenesMIPOL1, SLC25A21, 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)nsv1043410
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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