A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040371



Internal ID19129590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:90536846..90587886hg38UCSC Ensembl
Innerchr13:91189100..91240140hg19UCSC Ensembl
Innerchr13:89987101..90038141hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3851041
hg1951041
hg1851041
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713269
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)nsv1040371
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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