A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045611



Internal ID18788142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57058767..57778609hg38UCSC Ensembl
Innerchr15:57350965..58070807hg19UCSC Ensembl
Innerchr15:55138257..55858099hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38719843
hg19719843
hg18719843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3717936
Samples
Known GenesCGNL1, GCOM1, LINC00926, MYZAP, POLR2M, TCF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045611
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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