A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053686



Internal ID18796217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97119353..97150042hg38UCSC Ensembl
Innerchr13:97771607..97802296hg19UCSC Ensembl
Innerchr13:96569608..96600297hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3830690
hg1930690
hg1830690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525516
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)nsv1053686
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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