A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039164



Internal ID19128383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109645834..109666766hg38UCSC Ensembl
Innerchr13:110298181..110319113hg19UCSC Ensembl
Innerchr13:109096182..109117114hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3820933
hg1920933
hg1820933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525578
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)nsv1039164
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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