A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045474



Internal ID18788005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24144949..24297074hg38UCSC Ensembl
Innerchr15:24390096..24542221hg19UCSC Ensembl
Innerchr15:21941189..22093314hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38152126
hg19152126
hg18152126
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2423n100
Supporting Variantsnssv3540452
Samples
Known GenesPWRN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045474
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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