A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037339



Internal ID19126558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:57349867..57489367hg38UCSC Ensembl
Innerchr15:57642065..57781565hg19UCSC Ensembl
Innerchr15:55429357..55568857hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38139501
hg19139501
hg18139501
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n100
Supporting Variantsnssv3553591, nssv3553590
Samples
Known GenesCGNL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037339
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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