A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044215



Internal ID19133434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103011595..103034038hg38UCSC Ensembl
Innerchr13:103663945..103686388hg19UCSC Ensembl
Innerchr13:102461946..102484389hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3822444
hg1922444
hg1822444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525540
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044215
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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