A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044029



Internal ID18786560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:24113151..24303833hg38UCSC Ensembl
Innerchr15:24358298..24548980hg19UCSC Ensembl
Innerchr15:21909391..22100073hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38190683
hg19190683
hg18190683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2423n100
Supporting Variantsnssv3540321
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)nsv1044029
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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