A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048036



Internal ID18790567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:105463559..105534128hg38UCSC Ensembl
Innerchr13:106115908..106186477hg19UCSC Ensembl
Innerchr13:104913909..104984478hg18UCSC Ensembl
Cytoband13q33.2
Allele length
AssemblyAllele length
hg3870570
hg1970570
hg1870570
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525563
Samples
Known GenesDAOA, DAOA-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048036
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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