A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045291



Internal ID19134510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103077307..103123649hg38UCSC Ensembl
Innerchr13:103729657..103775999hg19UCSC Ensembl
Innerchr13:102527658..102574000hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3846343
hg1946343
hg1846343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525541
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)nsv1045291
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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