A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038016



Internal ID18780547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98665177..98817733hg38UCSC Ensembl
Innerchr13:99317431..99469987hg19UCSC Ensembl
Innerchr13:98115432..98267988hg18UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38152557
hg19152557
hg18152557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713287
Samples
Known GenesDOCK9, SLC15A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038016
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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