A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050235



Internal ID19139454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30152061..30376369hg38UCSC Ensembl
Innerchr15:30444264..30668572hg19UCSC Ensembl
Innerchr15:28231556..28455864hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38224309
hg19224309
hg18224309
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2501n100
Supporting Variantsnssv3546485, nssv3546484, nssv3546486
Samples
Known GenesCHRFAM7A, DKFZP434L187
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050235
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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