A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037215



Internal ID19126434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109206302..109351682hg38UCSC Ensembl
Innerchr13:109858650..110004029hg19UCSC Ensembl
Innerchr13:108656651..108802030hg18UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38145381
hg19145380
hg18145380
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713304
Samples
Known GenesMYO16
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037215
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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