A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528628



Internal ID18480223
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 StatusS
Merged Variantsnsv1043410
Supporting Variants
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)nssv3528628
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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