A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040554



Internal ID19129773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103444213..103514911hg38UCSC Ensembl
Innerchr13:104096563..104167261hg19UCSC Ensembl
Innerchr13:102894564..102965262hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3870699
hg1970699
hg1870699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1734n100
Supporting Variantsnssv3525544
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)nsv1040554
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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