A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052902



Internal ID18795433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41577079..41659374hg38UCSC Ensembl
Innerchr15:41869277..41951572hg19UCSC Ensembl
Innerchr15:39656569..39738864hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3882296
hg1982296
hg1882296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552258
Samples
Known GenesTYRO3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052902
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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