A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051686



Internal ID19140905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109631121..109710607hg38UCSC Ensembl
Innerchr13:110283468..110362954hg19UCSC Ensembl
Innerchr13:109081469..109160955hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3879487
hg1979487
hg1879487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525577
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)nsv1051686
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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