A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050626



Internal ID19139845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103007055..103024703hg38UCSC Ensembl
Innerchr13:103659405..103677053hg19UCSC Ensembl
Innerchr13:102457406..102475054hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3817649
hg1917649
hg1817649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525539
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)nsv1050626
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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