A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049015



Internal ID19138234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:101955072..101984810hg38UCSC Ensembl
Innerchr13:102607422..102637160hg19UCSC Ensembl
Innerchr13:101405423..101435161hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3829739
hg1929739
hg1829739
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525532
Samples
Known GenesFGF14, MIR2681
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049015
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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