A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040387



Internal ID19129606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30152061..30360018hg38UCSC Ensembl
Innerchr15:30444264..30652221hg19UCSC Ensembl
Innerchr15:28231556..28439513hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38207958
hg19207958
hg18207958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2501n100
Supporting Variantsnssv3546483
Samples
Known GenesDKFZP434L187
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040387
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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