A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036282



Internal ID19125501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73076493..73130123hg38UCSC Ensembl
Innerchr14:73543201..73596831hg19UCSC Ensembl
Innerchr14:72612954..72666584hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3853631
hg1953631
hg1853631
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531132
Samples
Known GenesRBM25
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036282
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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